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ORIGINAL RESEARCH article

Front. Pediatr., 23 September 2021
Sec. Obstetric and Pediatric Pharmacology
This article is part of the Research Topic Exploring Maternal-Fetal Pharmacology through PBPK Modeling Approaches View all 11 articles

Mechanistic Coupling of a Novel in silico Cotyledon Perfusion Model and a Physiologically Based Pharmacokinetic Model to Predict Fetal Acetaminophen Pharmacokinetics at Delivery

\nPaola Mian
Paola Mian1*Bridget Nolan,Bridget Nolan2,3John N. van den Anker,John N. van den Anker4,5Kristel van Calsteren,Kristel van Calsteren6,7Karel Allegaert,,Karel Allegaert6,8,9Nisha Lakhi,Nisha Lakhi2,3Andr DallmannAndré Dallmann10
  • 1Department of Clinical Pharmacy, Medisch Spectrum Twente, Enschede, Netherlands
  • 2Department of Obstetrics and Gynecology, Richmond University Medical Center, Staten Island, NY, United States
  • 3Department of Obstetrics and Gynecology, New York Medical College, Valhalla, NY, United States
  • 4Division of Clinical Pharmacology, Children's National Hospital, Washington, DC, United States
  • 5Department of Pediatric Pharmacology and Pharmacometrics, University Children's Hospital Basel, Basel, Switzerland
  • 6Department of Development and Regeneration, KU Leuven, Leuven, Belgium
  • 7Department of Gynecology and Obstetrics, UZ Gasthuisberg, Leuven, Belgium
  • 8Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium
  • 9Department of Hospital Pharmacy, Erasmus Medical Center Rotterdam, Rotterdam, Netherlands
  • 10Pharmacometrics/Modeling and Simulation, Research and Development, Pharmaceuticals, Bayer AG, Leverkusen, Germany

Little is known about placental drug transfer and fetal pharmacokinetics despite increasing drug use in pregnant women. While physiologically based pharmacokinetic (PBPK) models can help in some cases to shed light on this knowledge gap, adequate parameterization of placental drug transfer remains challenging. A novel in silico model with seven compartments representing the ex vivo cotyledon perfusion assay was developed and used to describe placental transfer and fetal pharmacokinetics of acetaminophen. Unknown parameters were optimized using observed data. Thereafter, values of relevant model parameters were copied to a maternal-fetal PBPK model and acetaminophen pharmacokinetics were predicted at delivery after oral administration of 1,000 mg. Predictions in the umbilical vein were evaluated with data from two clinical studies. Simulations from the in silico cotyledon perfusion model indicated that acetaminophen accumulates in the trophoblasts; simulated steady state concentrations in the trophoblasts were 4.31-fold higher than those in the perfusate. The whole-body PBPK model predicted umbilical vein concentrations with a mean prediction error of 24.7%. Of the 62 concentration values reported in the clinical studies, 50 values (81%) were predicted within a 2-fold error range. In conclusion, this study presents a novel in silico cotyledon perfusion model that is structurally congruent with the placenta implemented in our maternal-fetal PBPK model. This allows transferring parameters from the former model into our PBPK model for mechanistically exploring whole-body pharmacokinetics and concentration-effect relationships in the placental tissue. Further studies should investigate acetaminophen accumulation and metabolism in the placenta as the former might potentially affect placental prostaglandin synthesis and subsequent fetal exposure.

Introduction

Despite frequent and increasing drug use in pregnant women (1, 2), little is known about placental drug transfer and pharmacokinetics in the fetus. To address this knowledge gap, numerous physiologically based pharmacokinetic (PBPK) models for pregnant women were developed over the past years and used to simulate fetal pharmacokinetics (3, 4). Yet, adequate parameterization of placental drug transfer in these models remains challenging. While some models relied on various in vitro information, such as the drug's physicochemical properties or permeability across Caco-2 cell membranes, to estimate placental drug transfer (58), other models integrated kinetic data obtained from the ex vivo cotyledon perfusion assay (914) or fitted the placental permeability to clinical data (15).

The kinetic in silico models representing the ex vivo cotyledon perfusion system typically consist of few compartments and lump various tissue portions of the cotyledon, e.g., intravillous vascular, interstitial, and intracellular space, in a single compartment. Although in general these models appear to scale well with the placental drug transfer kinetics simulated in whole-body models, the relatively simple structure prevents a more mechanistic understanding of the transfer kinetics. For example, drug accumulation in the trophoblasts of the cotyledon—which may lengthen fetal drug exposure in vivo (16)—cannot be described by these models. Along the same line, the understanding of placental concentration-time profiles enables modeling concentration-effects profiles in the placental tissue, as the placenta is not only a ‘transfer' organ but an ‘active' organ with endocrine and metabolic functions. Hence, tissue-specific pharmacology of a given drug within the placenta and potential interactions with its endocrine synthesis and secretion of hormones (e.g., prostaglandins) may also affect fetal development and pregnancy outcome (e.g., preterm induction of labor).

In the obstetric clinical pharmacology field, pharmacokinetic data in pregnant women are sparse and data sharing can be an important step to advance the development and validation of PBPK models. Here, we used data on acetaminophen pharmacokinetics in the umbilical cord from two clinical studies (17, 18) to re-evaluate and refine a recently developed maternal-fetal PBPK model (13, 19). In our previous work, acetaminophen transfer across the placenta in the PBPK model was informed based on published data from the ex vivo cotyledon perfusion assay (20). Therefore, an in silico cotyledon perfusion model was previously developed to learn the transfer kinetics in the ex vivo cotyledon perfusion assay before implementing them in the PBPK model. However, the previously developed in silico cotyledon perfusion model consisted of 4 compartments only, namely the maternal and fetal reservoir and the maternal and fetal tissue portions of the cotyledon (13). It was therefore structurally different than the placental sub-structure implemented in the PBPK model (see Figures 1, 2) (19). Consequently, the parameters of the former model are not directly transferable to the latter and hence translatability across these models may not be guaranteed.

FIGURE 1
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Figure 1. Structure of the maternal-fetal PBPK model. Gray boxes represent compartments of the physiologically based pharmacokinetic (PBPK) model; solid arrows denote drug transport via the organ blood flow; dashed arrows denote drug transport via passive diffusion; dash dotted lines denote drug transport via gastrointestinal motility or the biliary excretion route.

FIGURE 2
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Figure 2. Structure of the placenta sub-model integrated in the maternal-fetal PBPK model. Gray boxes represent sub-compartments of the placenta structure implemented in the maternal-fetal physiologically based pharmacokinetic (PBPK) model; dash-dotted boxes represent the vascular space; solid arrows denote drug transport via the organ blood flow; and dashed arrows denote drug transport via passive diffusion. The maternal plasma and blood cell compartments represent the intervillous space, and the maternal interstitial and intracellular space represent the placental septae and the decidua basalis, respectively. The fetal intracellular compartment represents the (syncytio-)trophoblasts with the apical membrane facing the maternal plasma compartment and the basolateral membrane facing the fetal interstitial compartment. The fetal interstitial space represents intravillous fibrous tissue and the plasma and blood cell compartments represent the intravillous vascular system.

To this end, a novel in silico cotyledon perfusion model was developed herein that constitutes a congruent, albeit minimized, replicate of the placental structure implemented in the maternal-fetal PBPK model. Additionally, it was intended that the novel in silico cotyledon perfusion model better reflected the cotyledon physiology so that potential drug accumulation in the tissue could be considered in the simulations. Several parameters of the in silico cotyledon perfusion model relevant to maternal-fetal drug transfer were then optimized using previously published data for acetaminophen. The optimization results were then transferred into the PBPK model and the predicted pharmacokinetics in the umbilical vein at delivery were re-evaluate using the pooled data of Nitsche et al. (17) and Mehraban et al. (18).

Materials and Methods

Software

PBPK models were built with PK-Sim® and MoBi® which are available as open source tools through the Open Systems Pharmacology (OSP) software, version 9.1, via GitHub (https://github.com/Open-Systems-Pharmacology) (21). The software R, version 3.6.3 (R Foundation for Statistical Computing, http://www.r-project.org) was used for graphics creation and statistical analysis. The R-package “ospsuite”, version 9.0.79 (https://github.com/Open-Systems-Pharmacology/OSPSuite-R), was used to conduct pharmacokinetic simulations in virtual populations of pregnant women. The tool WebPlotDigitizer, version 4.0 (https://automeris.io/WebPlotDigitizer/) was used to extract data from figures and conversion into numerical format.

General Workflow

In our previous study, we successfully translated an adult, non-pregnant PBPK model for acetaminophen including its metabolites generated by uridine 5′-diphospho-glucuronosyltransferase (UGT) 1A1, sulfotransferase (SULT) 1A1 and cytochrome-P-450 (CYP) 2E1 to pregnancy (13, 19). The predicted acetaminophen pharmacokinetics in the maternal blood were previously verified in the first trimester with clinical data from Beaulac-Baillargeon and Rocheleau (22); predicted acetaminophen pharmacokinetics in the maternal and umbilical vein blood at delivery were previously evaluated with data from Allegaert et al. (23) and Nitsche et al. (17), respectively.

In this study, we developed a novel in silico cotyledon perfusion model that is structurally equivalent with the placenta implemented in the PBPK model. We used this in silico cotyledon perfusion model to learn placental transfer kinetics of acetaminophen by fitting relevant model parameters to observed data obtained in the ex vivo perfusion cotyledon assay (20). Once this model captured the observed ex vivo kinetics adequately, the values of relevant model parameters were copied to the maternal-fetal PBPK model. Note that the structure of the PBPK model was not changed in this study and is thus consistent with the structure of the PBPK model reported in our previous publication (13). Thereafter, fetal pharmacokinetics were predicted in the umbilical vein compartment of the PBPK model and predictions were evaluated with clinical data from Nitsche et al. (17) and Mehraban et al. (18).

In silico Cotyledon Perfusion Model

Description of the Model

A novel in silico cotyledon perfusion model structure, schematically depicted in Figure 3, was developed that closely reflects the physiological structure of the cotyledon ex vivo. Note that the maternal intracellular compartment representing mainly the decidua basalis is only present in the PBPK model, but not in the in silico cotyledon perfusion model. Since the decidua is shed off during childbirth, it is not part of the cotyledon tissue used in the ex vivo experiment and only present in utero. Although there will still be decidual remnants on the delivered placenta, they come off during flushing and rinsing for experimental preparation. Hence, the in silico cotyledon perfusion model consists of seven compartments: The maternal perfusate in the maternal reservoir and in the intervillous space of the cotyledon; the intervillous interstitial compartment representing fibrous tissue adhering to the cotyledon on the maternal-facing side; the trophoblasts; the interstitial space representing fibrous tissue in the fetal villous; and the fetal perfusate in the fetal villous and fetal reservoir. Table 1 gives an overview of the tissue components present in vivo/ex vivo and their corresponding compartments in the in silico cotyledon perfusion model (Figure 3) and the placental sub-structure of the PBPK model (Figure 2).

FIGURE 3
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Figure 3. Structure of the ex vivo cotyledon perfusion model. Boxes represent compartments of the novel ex vivo cotyledon perfusion model and solid arrows denote drug transport via the perfusate flow or diffusion. The cotyledon is highlighted as dashed box.

TABLE 1
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Table 1. Overview of different tissue components and their corresponding compartments in the novel in silico cotyledon perfusion model and the PBPK model.

The ordinary differential equations (ODE) given in the following were used in the novel in silico cotyledon perfusion model. Note that in MoBi®, the ODEs are first defined for intercompartmental exchange processes in the passive transports building block; during set-up of a simulation, the ODEs are then generated for each compartment. In the following, the ODEs are first introduced for each intercompartmental exchange transport and then defined for the compartments.

The following equations were used to describe drug transfer in perfusate between the maternal reservoir and the cotyledon (Equation 1) and between the fetal reservoir and the cotyledon (Equation 2):

dNM_perfdt=QM×(CM_res-CM_perf)    (1)
dNF_perfdt=QF×(CF_res-CF_perf)    (2)

Here, NM_perf and NF_perf denote the molar drug amount in the maternal and fetal perfusate, respectively, that fills the intervillous space of the cotyledon [μmol]; QM and QF denote the flow rate of the perfusate in maternal and fetal system, respectively [L/min]; CM_res and CF_res the molar drug concentration in maternal and fetal perfusate in the reservoir, respectively [μmol/L]; and CM_perf and CF_perf the molar drug concentration in maternal and fetal perfusate in the cotyledon, respectively [μmol/L]. QM and QF as well as the volumes of the maternal and fetal reservoirs were set to the values reported by Conings et al. (20); 14 mL/min and 6 mL/min for the flow rate in the maternal and fetal system, respectively; and 280 and 284 mL for the maternal and fetal reservoir volume. Drug amount was converted to drug concentration by dividing the drug amount by the compartment's volume.

Drug transfer between maternal perfusate in the cotyledon and intervillous interstitial space and fetal perfusate in the cotyledon and intravillous interstitial space was described by Equations 3, 4, respectively:

dNM_intM_intM_perfdt=fu×Pendo×SAM_perf : int×(CM_perf-CM_intKM_int : perf)    (3)
dNF_intF_intF_perfdt=fu_fetus×Pendo×SAF_perf : int×(CF_perf-CF_intKF_int : perf)    (4)

Here, NM_intM_intM_perf denotes molar drug amount in the intervillous interstitial compartment when drug exchange is only considered to occur between the intervillous interstitial space and maternal perfusate in the cotyledon [μmol]; NF_intF_intF_perf denotes molar drug amount in the intravillous interstitial compartment when drug exchange is only considered to occur between the intravillous interstitial space and fetal perfusate in the cotyledon [μmol]; fu and fu_fetus denote the drug's fraction unbound in maternal and fetal perfusate, respectively; Pendo is the drug's permeability through the endothelial membrane of blood vessels and was assumed to be equal for maternal and fetal endothelial membranes [dm/min]; SAM_perf : int and SAF_perf : int denote the surface area between maternal perfusate and intervillous interstitial space and fetal perfusate and intravillous interstitial space, respectively [dm2]; CM_int and CF_int the molar drug concentration in intervillous and intravillous interstitial space of the cotyledon, respectively [μmol/L]; KM_int : perf is the intervillous interstitial-to-perfusate partition coefficient of the drug; and KF_int : perf is the intravillous interstitial-to-perfusate partition coefficient of the drug.

The unbound fraction of acetaminophen was scaled from an adult value of 0.82 (19) as described previously (24). The bovine serum albumin concentrations present in the maternal and fetal perfusate of the ex vivo cotyledon perfusion assay were 40 and 30 mg/mL, respectively (20). This resulted in an unbound fraction of 0.84 and 0.88 in maternal and fetal perfusate, respectively. Permeability across the endothelial membrane in the intervillous and intravillous space (Pendo) was assumed to be not the rate-limiting step for tissue distribution and was hence set to a value of 100 cm/min as has been done for other organ compartments (except the brain) in whole-body PBPK models (24). Note that for drugs that are substrates to efflux transporters expressed in the endothelial membrane, this rate may have to be reduced. SAM_perf : int and SAF_perf : int were estimated by scaling the local surface area from the cotyledon volume assuming that organ structure is geometrically similar among species (24). The volumes of the intervillous and intravillous cotyledon fraction were assumed to be 23 and 35 mL, respectively (25). KM_int : perf was calculated from the biochemical tissue composition of the cotyledon and the drug's physicochemical properties using the equation published by Schmitt (26). Values for the biochemical composition of the placenta have been reported previously (27). Finally, KF_int : perf was calculated accordingly, except that the fraction unbound in the original equation by Schmitt (26) was replaced by the fetal fraction unbound (Equation 5):

KF_int : perf=(fwaterint+fproteinintfproteinperf×(1fu_fetus-fwaterperf))×fu_fetus    (5)

In this equation, fwaterint and fwaterperf denote the fractional water content in intravillous interstitial space and perfusate, respectively; and fproteinint and fproteinperf the fractional protein content in intravillous interstitial space and perfusate, respectively. fwaterint was assumed to be the same than for the intervillous interstitial space [0.935 (28)] and fwaterperf was assumed to be similar to the fractional volume content reported for plasma [0.926 (28)]. The value for the ratio fproteinintfproteinperf in the ex vivo cotyledon was assumed to be the same as in adult tissue [0.37 (26)].

Intravillous drug transfer between interstitial and intracellular space (i.e., the trophoblasts) was described by Equation 6:

dNF_cellF_cellF_intdt = P×SAF_int : cell×                                               (KF_water : int×CF_int KF_water : cell×CF_cell)    (6)

Here, NF_cellF_cellF_int denotes molar drug amount in the intracellular space when drug exchange is only considered to occur between the intracellular and intravillous interstitial compartment [μmol]; P is the drug's membrane permeability [dm/min] which was calculated from the drug's effective molecular weight and lipophilicity as described elsewhere (24); SAF_int : cell is the surface area between the intravillous interstitial space and the intracellular space (i.e. trophoblasts) [dm2]; KF_water : int the partition coefficient between water and intravillous interstitial space; KF_water : cell the partition coefficient between water and intracellular space of the trophoblasts; and CF_cell the molar drug concentration in the trophoblasts [μmol/L]. The local surface area in this equation was calculated as already described above. KF_water : int and KF_water : cell were expressed as follows:

KF_water : int=fu_fetusKF_int : perf    (7)
KF_water : cell=fu_fetusKF_cell : perf    (8)

where KF_int : perf is calculated according to the Equation 5 and KF_cell : perf according to the cell-to-plasma partition coefficient equation. In the developed in silico cotyledon perfusion model, several equations were implemented to calculate these partition coefficients from the biochemical tissue composition of the placenta (27) and the drug's physicochemical properties using, namely the PK-Sim Standard equation (29) and the equations proposed by Schmitt et al. (26), Rodgers et al. (30, 31), and Poulin et al. (32, 33). For acetaminophen, the partition coefficient equation by Rodgers et al. (30, 31) was used. Note that in the presented model, KF_cell : perf was included as global parameter that used per default the maternal fraction unbound; to correct for the fetal fraction unbound, KF_cell : perf was multiplied by the ratio of fetal-to-maternal fraction unbound. Hence, inserting Equations 5, 7, 8 into Equation 6 as well as correcting for the fetal fraction unbound yields Equation 9 which was implemented in the model:

dNF_cellF_cellFintdt=P×SAF_int : cell×(CF_int×(fwaterint+fproteinintfproteinperf×(1fu_fetus-fwaterperf))-1)(-CF_cell×fu_fetusKF_cell : perf×fu_fetusfu)    (9)

Or, alternatively and in a shorter form (Equation 10):

dNdt = P×SAF_int : cell              ×(CF_int×fu_fetusKF_int : perfCF_cell×fuKF_cell : perf)    (10)

Finally, maternal-fetal drug transfer across the apical side of the trophoblast was modeled between maternal perfusate in the intervillous space and the trophoblasts using Equation 11:

dNF_cellF_cellM_perfdt = P×SAvilli×fu                                                   ×(fin×CM_perffout×CF_cellKFM_cell : perf)    (11)

In this equation, NF_cellF_cellM_perf denotes molar drug amount in the intracellular space when drug exchange is only considered to occur between the intracellular space and maternal perfusate in the cotyledon [μmol]; SAvilli is the surface area of the fetal villi at the interface of maternal perfusate in the cotyledon and trophoblasts [dm2]; fin and fout are factors modifying the influx and efflux permeability of the drug (i.e. in maternal→fetal and fetal→maternal direction), respectively; and KFM_cell : perf is the drug's partition coefficient between fetal intracellular space (trophoblasts) and maternal perfusate in the cotyledon.

Per default, fin and fout in Equation 11 are set to 1 (i.e. equal permeability in both directions). SAvilli was estimated by diving the absolute surface area of all fetal villi in the term placenta, ~1178 dm2 (27), by the average number of cotyledons in the placenta which varies around 35 at term (34). The drug's permeability across the trophoblasts' membrane was calculated from the drug's effective molecular weight and lipophilicity as described elsewhere (24) resulting in a value of 4.29 · 10−2 cm/min for acetaminophen. KFM_cell : perf was estimated as described above, i.e. according to the method described by Rodgers et al. (30, 31). Of note, the value of KFM_cell : perf in Equation 11 is similar to that of KF_cell : perf in Equation 10 because both partition coefficients refer to the same intracellular compartment (trophoblast). KFM_cell : perf is located at the apical membrane and KF_cell : perf at the basolateral membrane of the trophoblasts.

Hence, combining the ODEs above for the specific intercompartmental exchange processes gives the full ODE system of the novel in silico cotyledon perfusion model:

dt[NM_resNM_perfNM_intNF_cellNF_intNF_perfNF_res]=E[CM_resCM_perfCM_intCF_cellCF_intCF_perfCF_res]    (12)

Here, N and C denote molar drug amount [μmol] and molar drug concentration [μmol/L] in the compartment specified by the subscript and E describes the intercompartmental drug exchange processes that have been specified in Equations 1–11. More specifically, E can be written as the following 7 × 7 matrix:

E=[QMQM0QMQMfu×(Pendo×SAM_perf:int+P×SAvilli×fin)Pendo×SAM_perf:int×fu0Pendo×SAM_perf:int×fuPendo×SAM_perf:int×fuKM_int:perf0P×SAvilli×fin×fu00000000000000P×SAvilli×fout×fuKF_cell:perf0000000P×fu×(fout×SAvilliKFM_cell:perf+SAF_int:cellKF_cell:perf)P×SAF_int:cell×fu_fetusKF_int:perf00P×SAF_int:cell×fuKF_cell:perffu_fetusKF_int:perf×(P×SAF_int:cell+Pendo×SAF_perf:int)Pendo×SAF_perf:int×fu_fetus00Pendo×SAF_perf:int×fu_fetusKF_int:perfQFPendo×SAF_perf:int×fu_ftus000QFQF]    (13)

Model Optimization

After the model has been implemented as described above, it was used to simulate acetaminophen concentrations in the maternal and fetal reservoir. Model parameters relevant for placental drug transfer, namely fin, fout and the placental partition coefficients (KFM_cell : perf on the apical side and KF_cell : perf on the basolateral side of the trophoblast), were optimized to better capture the observed data reported by Conings et al. (20). More specifically, the following optimization scenarios were tested:

• Optimizing symmetrical drug transfer: fin and fout were both fitted together so that the permeability in maternal→fetal and fetal→maternal direction was modified by the same factor.

• Optimizing asymmetrical drug transfer: fin and foutwere fitted separately from each other, resulting in different permeability values in maternal→fetal and fetal→maternal direction.

• Optimizing symmetrical drug transfer and the placental partition coefficients: In addition to fitting fin and fout together, KFM_cell : perf and KF_cell : perf were also fitted together (i.e. both partition coefficients had the same fitted value). Hence, the permeability in maternal→fetal and fetal→maternal direction was modified by the same factor as were the partition coefficients. Fitting KFM_cell : perf and KF_cell : perf facilitated changes in intracellular drug concentrations (e.g., causing drug accumulation in the trophoblasts).

• Optimizing asymmetrical drug transfer and the placental partition coefficients: fin and fout were fitted separately from each other, while KFM_cell : perf and KF_cell : perf were fitted together (i.e. both partition coefficients had the same fitted value). This resulted in different permeability values in maternal→fetal and fetal→maternal direction and in modified additionally intracellular drug concentrations.

Parameter optimizations were conducted using the built-in module in MoBi® and the Monte-Carlo algorithm. All observed data [in total 18 data sets comprising 455 data values (20)] were included in the parameter optimization.

Fetal-Maternal PBPK Model for Acetaminophen

Description of the Model

After training the novel in silico cotyledon perfusion model to learn placental transfer kinetics of acetaminophen from the ex vivo cotyledon perfusion data, the fitted parameter values were copied to the PBPK model to predict acetaminophen pharmacokinetics in the umbilical vein at delivery. The structure of this whole-body model is schematically shown in Figure 1 and the sub-structure of the placenta implemented in that model is depicted in Figure 2. In this placental sub-structure, the maternal plasma and blood cell compartments represent together the intervillous space, the maternal interstitial represents the placental septae and the maternal intracellular space represents the decidua basalis which is distorted during labor-induced contraction of the myometrium and eventually destroyed by the hemorrhages during delivery. The fetal intracellular compartment represents the (syncytio-)trophoblasts with the apical membrane facing the maternal plasma compartment and the basolateral membrane facing the fetal interstitial compartment. The fetal interstitial space represents intravillous fibrous tissue and the plasma and blood cell compartments represent the intravillous vascular system.

The PBPK model was corrected for the drug's unbound fraction in fetal compartments. Unbound maternal and fetal fraction of acetaminophen were calculated from the albumin plasma concentrations using a previously reported function (24). For the mother, albumin plasma concentrations were calculated for each patient's gestational age (27), while for the fetus, a concentration of 32 g/L was used as has been reported for the gestational age range from 35 to 38 weeks (35). Placental transfer parameters in the PBPK model were replaced with the fitted values from the in silico cotyledon perfusion model (see section Model Optimization). Of note, while the permeability across the placenta in the PBPK model was the same as in the in silico cotyledon perfusion model (4.29 · 10−2 cm/min), the transfer rate in the PBPK model was scaled with the villi surface area resulting thus in a larger transfer clearance for the total placenta compared to the cotyledon. All other model parameters were kept the same as published previously (13, 19).

Model Simulations

Pharmacokinetics were predicted in the venous plasma of the umbilical cord. For each patient, a virtual population of 100 pregnant women with the patient's body weight and height as well as gestational week was created using the population creation algorithm of the R-package ‘ospsuite'. Unfortunately, the study by Nitsche et al. (17) did not report the individual body weight and height of each patient and, thus, a virtual population with standard body weight at term delivery (24) was used for the simulations. The population simulation results for all patients were pooled for calculation of the overall median and percentiles and for further analysis.

Patients and Data

Nitsche et al. (17) studied maternal and fetal pharmacokinetics in 34 women without medical or obstetrical complications following a single oral dose of 1,000 mg acetaminophen upon admission for scheduled cesarean delivery. Patient characteristics are listed in Table 2. Pharmacokinetic data were extracted from the concentration-time profile figure published by Nitsche et al. (17). From the 34 women, only 28 data values could be extracted.

TABLE 2
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Table 2. Patient characteristics.

Additional concentration data in the umbilical cord were obtained from the study by Mehraban et al. (18). From the 121 patients with intrapartum fever of whom blood samples were collected in this study, we included the 45 patients who received a single oral dose of 1,000 mg acetaminophen. Two additional patients were excluded from our analysis because of unusually high acetaminophen concentrations in the umbilical cord which we attributed to documentation errors (the umbilical vein concentrations of these patients were 14.5 and 3.1 mg/L at 18 and 55 h after dose administration). Characteristics of the patients included in our analysis are listed in Table 2.

Few measured concentrations in the study by Mehraban et al. (18) fell below the lower limit of quantification (LLOQ). These data were included as LLOQ/2 in this analysis. It has to be noted that in the study by Mehraban et al. (18), maternal concentrations were not measured.

PBPK Model Evaluation

Predicted concentrations in the umbilical vein were visually compared to clinical data obtained from clinical studies. Additionally, goodness-of-fit plots depicting predicted vs. observed concentrations and residuals vs. time plots were created and the mean prediction error (MPE) and mean absolute prediction error (MAPE) were calculated.

Ethics

Ethics and study registration related aspects are clearly mentioned in the original publications (17, 18) that served as source of this refinement effort, and no additional registration or procedures were needed.

Results

In silico Cotyledon Perfusion Model

Of the four tested optimization scenarios, optimizing asymmetrical drug transfer and the placental partition coefficients yielded the lowest simulation error. The fitted value ± 95% confidence interval for the placental partition coefficients, KFM_cell : perf and KF_cell : perf, was 4.31 ± 0.57 [vs. 0.76 when being estimating according to the method described by Rodgers et al. (30, 31)] resulting in a substantial amount of acetaminophen accumulating in the trophoblasts of the cotyledon.

The fitted values ± 95% confidence intervals for fin and fout were 0.060 ± 0.0058 and 0.051 ± 0.0061, respectively. This resulted in permeability values in maternal→fetal and fetal→maternal direction of 2.56 × 10−3 and 2.18 × 10−3 cm/min, respectively, vs. 4.29 × 10−2 cm/min when the permeability was estimated from the physicochemical properties of acetaminophen. Figure 4 presents the observed and simulated concentration-time profiles of acetaminophen in maternal and fetal perfusate in the reservoirs of the ex vivo cotyledon perfusion assay.

FIGURE 4
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Figure 4. Observed and simulated concentration time profiles in the novel ex vivo cotyledon perfusion model. In each experiment, acetaminophen was either administered to the fetal reservoir (A–D) or maternal reservoir (E–N) at time = 0h. The initial concentration was 10 mg/L in all experiments (to reflect clinically relevant concentrations); each panel refers to an individual experiment. All experiments were conducted under similar conditions. Observed data were taken from Conings et al. (20).

The results of a local sensitivity analysis are presented in Figure 5. In this figure, simulation results are shown when KFM_cell : perf and KF_cell : perf were set to 0.76 [i.e., the value estimated according to the method described by Rodgers et al. (30, 31)], 2.5, and 4.31 (i.e., the fitted value). All other model parameter values were kept unchanged in this sensitivity analysis. Pooled over all individual experiments, the MPE was 375%, 131, and −62.6% when using placental partition coefficient values of 0.76, 2.5, and 4.31, respectively.

FIGURE 5
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Figure 5. Local sensitivity analysis for the placental partition coefficients (KFM_cell : perf and KF_cell : perf). In each experiment, acetaminophen was either administered to the fetal reservoir (A–D) or maternal reservoir (E–N) at time = 0 h. The initial concentration was 10 mg/L in all experiments (to reflect clinically relevant concentrations); each panel refers to an individual experiment. All experiments were conducted under similar conditions. Observed data were taken from Conings et al. (20).

PBPK Model Evaluation

Figure 6 presents the concentration-time profile predicted in the umbilical vein together with the clinical data reported by Nitsche et al. (17) and Mehraban et al. (18). The observed inter-individual variability, especially in the data reported by Mehraban et al. (18), was considerably larger than the predicted variability. For the pooled data sets, MPE and MAPE were 24.7 and 68.7%, respectively. For the data reported by Nitsche et al. (17), MPE and MAPE were −10.4 and 29.9%, respectively; and for the data reported by Mehraban et al. (18), MPE and MAPE were 49.3 and 96.0%, respectively.

FIGURE 6
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Figure 6. Concentration time profiles for acetaminophen in the umbilical cord. Blue and red circles indicate observed clinical data reported by Nitsche et al. (17) and Mehraban et al. (18). Data from Mehraban et al. (18) below the lower limit of quantification (LLOQ), shown as dashed line, are included as LLOQ/2 and empty circles in the figure. The black line indicates the predicted median and the shaded area the predicted 5–95th percentile range.

Figure 7 presents the goodness-of-fit plot and the residuals plotted against time. For the pooled data sets, 50 (81%) out of 62 concentration values were predicted within a 2-fold error range (excluding values below LLOQ). For the data reported by Nitsche et al. (17), 25 (89%) out of 28 concentrations were predicted within the 2-fold error range, whereas for the data reported by Mehraban et al. (18), 25 (74%) out of 34 concentrations that were above LLOQ were predicted within that range.

FIGURE 7
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Figure 7. Goodness-of-fit plot (A) and residuals versus time plot (B) for the predicted acetaminophen concentrations in the umbilical vein. Blue and red circles indicate clinical data reported by Nitsche et al. (17) and Mehraban et al. (18). Data from Mehraban et al. (18) below the lower limit of quantification (LLOQ) are included as LLOQ/2 and empty circles in the figure. In (A), the solid line indicates the line of identity and the dashed lines limit the 2-fold error range. In (B), the solid line indicates the level where the residuals are zero.

Discussion

The ex vivo cotyledon perfusion assay is often used to quantify drug transfer across the placenta and the results obtained from this assay can be leveraged in a PBPK modeling framework (36). While the previously developed in silico cotyledon perfusion model for acetaminophen directly links maternal with fetal perfusate (13), the PBPK model separates maternal from fetal blood plasma by interposing the fetal intracellular compartment (representing the trophoblasts) and the fetal interstitial compartment (representing stroma tissue in the fetal villi) (19). Owing to these structural differences, parameters in the in silico cotyledon perfusion model did not translate directly to parameters in the PBPK model. For example, the partition coefficient between maternal and fetal perfusate in the former model did not have an equivalent parameter in the PBPK model. Hence, this study aimed at developing an in silico cotyledon perfusion model with a more physiologic representation of the cotyledon and a compartmentalization of different tissue portions. Subsequently, this model was optimized to simulate published data for acetaminophen (20). Several parameters relevant to maternal-fetal drug transfer were optimized in this model and the best optimization results were then transferred into a previously developed whole-body PBPK model for acetaminophen (13, 19) to predict pharmacokinetics in the umbilical vein at delivery. The predictive performance of the PBPK model was then assessed with clinical data reported by Nitsche et al. (17) and Mehraban et al. (18).

The developed in silico cotyledon perfusion model consisted of seven compartments (Figure 3). It could be argued that the fetal compartment is missing the fetal endothelial cells since they represent an additional barrier to diffusion into the fetal plasma and blood cells which may become relevant, especially when it constitutes the rate-limiting step for drug distribution into the fetal reservoir. In this case, this barrier could be technically simulated by reducing the permeability across the endothelial membrane in the intravillous space (Pendo). This also applies to drugs that are substrates to efflux transporters expressed in the endothelial membrane. While the transfer rate across the endothelial cells could be technically simulated, drug accumulation in the endothelial cells cannot be described by this model. For this case, a structural refinement of the model is necessary.

Data measured in the ex vivo cotyledon perfusion assay for acetaminophen (20) were used to optimize the model so that the observed data could be adequately reproduced (Figure 4). Obviously, the volume of the cotyledon [23 and 35 mL for the intervillous and intravillous cotyledon fraction, respectively (25)] appeared not always correctly parameterized since some simulations overestimated the observed concentrations at time point zero (see e.g., Figure 4E), although experimental sampling or measurement errors could also have given rise to these deviations.

It was observed that when increasing the placental partition coefficients, steady state acetaminophen concentrations in the maternal and fetal reservoir were slightly better simulated as indicated by the lower MPE, although the overall effect of higher placental partition coefficients on the concentrations in the reservoirs was rather small (Figure 5). The results of the sensitivity analysis (Figure 5) indicated that the measured acetaminophen concentrations in the maternal and fetal reservoirs were somewhat sensitive when accumulation in the trophoblasts was increased. Hence, the information content in these data was rather limited and results should be interpreted considering this uncertainty. Even though some uncertainty with respect to acetaminophen accumulation in the trophoblasts remains, the model simulations, especially the simulated steady state concentrations in the reservoirs, improved when acetaminophen was, at least to some extent, ‘removed' from the reservoirs by either shifting it into other compartments (e.g., the trophoblasts) or completely removing it from the system. In the ex vivo experiment, this could have been caused by either accumulation in the cotyledon, by binding to the experimental equipment (e.g., the inner wall of the tubes) or by the loss of acetaminophen due to e.g., the sampling procedure or metabolism in the cotyledon. Here, rather than modeling acetaminophen metabolism, the partition coefficients KFM_cell : perf and KF_cell : perf were fitted allowing an accumulation in the trophoblasts. The fitted value (4.31) indicated that simulated acetaminophen concentrations at steady state are more than 4-fold greater in the trophoblasts vs. the maternal perfusate. Although various clinical studies have shown that several drugs accumulate in placental tissue, including ciprofloxacin (37), sildenafil (38), and tacrolimus (39), it is unclear whether acetaminophen also accumulates in placental tissue. If so, acetaminophen might affect prostaglandin synthesis in the placenta, and subsequent fetal exposure with potentially deleterious effects on fetal development, future studies may further investigate this point.

However, metabolism could, at least partly, also be an explanation why the amount of acetaminophen in the maternal and fetal perfusate at steady state was lower than initially expected. Acetaminophen is predominantly metabolized by members of the UGT1A subgroup (mainly UGT1A1), members of the SULT1A subgroup (mainly SULT1A1), whereas a very minor extent is metabolized by CYP1A2, 2E1 and 3A4 to the toxic metabolite N-acetyl-p-benzoquinone imine (NAPQI). Although expression studies show somewhat conflicting results, it appears that most of these enzymes, including UGT1A, CYP1A2, and CYP2E1, can only be detected in placentae collected in the first trimester, but not in term placentae, whereas CYP3A4 is expressed, but apparently not functionally active in the term placenta (40, 41). SULT1A was reported to be expressed and active in the term placenta (42). However, Conings et al. (20) observed that during ex vivo cotyledon perfusion experiments with acetaminophen, the phase II metabolites acetaminophen glucuronide and sulfate could not be detected, whereas in perfusion experiments with acetaminophen glucuronide and sulfate, back-conversion to acetaminophen (deglucuronidation and desulfation) seemed to occur. Hence, placental metabolism of acetaminophen—and the potential conversion of phase II metabolites to the parent compound—is currently poorly understood. This aspect should be further investigated in future studies to disentangle acetaminophen accumulation and metabolism in the placenta as well as formation from its phase II metabolites. Accounting (even partially) for metabolism could improve the value of the model. This issue could potentially be addressed more specifically when selecting another drug with a better characterization of its placental metabolism profile.

The presented model enables to explore the concentration-time and concentration-effect profiles in placental tissue. To illustrate the relevance of this construct, with acetaminophen as example, we should be aware that the placenta is also a highly active secreting endocrine organ. This includes prostaglandins secreted to the fetal circulation to ensure high prostaglandin exposure throughout fetal life. In the event of transient placental acetaminophen accumulation, it is likely that this will affect prostaglandin synthesis, and subsequent fetal exposure. This may provide additional insight in the side effects associated with maternal acetaminophen (neurodevelopmental, fetal patent ductus constriction, atopy, fertility) intake during pregnancy, in addition or besides the subsequent fetal acetaminophen exposure (4346). Finally, the concept of accumulation in placental tissue as observed for different compounds, and integrated in the current PBPK model should stimulate researchers to also consider conducting ex vivo cotyledon perfusion studies in both naïve as well as in placentas already exposed to a given compound before delivery.

The maternal-fetal PBPK model was used in a second step to predict acetaminophen concentrations in the umbilical cord at delivery. It was assumed that, apart from the pregnancy-induced physiological changes, neither labor nor the patient's condition (e.g., intrapartum maternal fever) would influence acetaminophen pharmacokinetics. The only adjustment related to labor and/or drugs administered in the peripartum period, such as opioids, was the 3-fold increase in gastric emptying time in the model as discussed previously (13). While all patients in the dataset by Mehraban et al. (18) received epidurals, pharmacokinetic data for the mother were not measured. The maternal pharmacokinetic data reported by Nitsche et al. (17) suggest that a 3-fold increase in gastric emptying time in the PBPK model is adequate to capture the data (13). Similar findings were also reported by Mendes et al. (9), although the authors changed the absorption rate and not gastric emptying time in their PBPK model.

The prediction results indicated that acetaminophen pharmacokinetics in the umbilical vein were overall satisfactory (Figure 6). However, inter-individual variability was substantially underestimated. This findings is not surprising because the physiological variability implemented in the PBPK model was derived from healthy pregnant women who were not in labor (27). Obviously, relatively little data is available that quantifies inter-individual variability in relevant physiological parameters (gastric emptying, organ blood flows, glomerular filtration rate etc.) during labor and hence the integration of physiological variability in PBPK models can at best be driven by plausible assumptions that are subsequently evaluated with clinical data. The predicted median concentration-time profile captured the observed data reasonably, though, as indicated by the relatively small MPE of 25.9%. Future studies should hence focus on reasonably capturing the large variability. This might also help assessing whether e.g., the two patients excluded from this analysis should really be treated as outliers (or documentation errors) or whether the unusually high concentrations from these patients could be attributed to e.g., variations in placental permeability as a consequence of labor, concomitant drug intake and/or diseases.

Unfortunately, observed maternal concentration data were not available for all patients. Such data could have helped better identifying the reasons why for some patients the fetal concentrations were rather poorly predicted. For example, a relatively large proportion of the fetal concentrations reported by Mehraban et al. (18) fell below the LLOQ. Without corresponding maternal data, is it difficult to determine whether acetaminophen poorly crossed the placenta barrier in these patients or whether maternal pharmacokinetics (e.g., delayed absorption or very fast metabolism) were responsible for the low fetal concentrations. A disease-related effect on placental drug transfer might, at least to some extent, explain the low concentrations in the umbilical cord. From the 43 patients included in this analysis, three were hypertensive and four additional patients were diabetic. Both conditions appear to be associated with impaired uteroplacental blood flow (47, 48). Additionally, it has been found that placentae from pregnancies complicated by gestational diabetes, especially if poorly controlled, show a decrease in the fluidity and a thickening of the syncytiotrophoblasts' membrane (4951). These alterations could, at least partly, reduce placental drug transfer. In fact, from the seven hypertensive or diabetic patients included in this analysis, five umbilical cord samples yielded concentrations below the LLOQ, whereas the concentrations from the other hypertensive or diabetic patients did not appear to differ from the remaining data. Interestingly, although one of the two patients excluded from this analysis was also suffering from gestational hypertension, the umbilical cord concentration obtained from this patient was unusually high (3.1 mg/L at 55 h) which seems inconsistent with a reduced placental drug transfer. Still, these considerations illustrate that the influence of diseases on the physiology in pregnant women should ideally be integrated in PBPK models, if applied to a clinical setting.

Several limitations pertain to the presented findings and models. In the in silico cotyledon perfusion model, many parameters could not be adequately identified, and hence biologically plausible assumptions had to be made. For example, the biochemical tissue composition of the placenta and cotyledon—a relevant input parameter for estimating the partition coefficients—was assumed to be similar. Currently, information is lacking in the scientific literature that would allow are more detailed discrimination of the biochemical composition of intervillous and intravillous structures in the placenta. Also, enzyme expression and drug metabolism in the placenta was not accounted for in the models. Kinetic data of acetaminophen metabolites measured in the ex vivo cotyledon perfusion assay could be used to assess enzyme abundance in the placenta, although this is complicated by the apparent back-conversion of metabolites to the parent compound (20). Additionally, results of the parameter optimization suggested some identification difficulties when fitting the parameters. In fact, fin and fout showed a relative strong correlation with the partition coefficients indicating that either the permeability or the partitioning should be ideally fixed to avoid non-identification issues. Further studies are needed to better inform these parameter separately.

In conclusion, this study presents a novel in silico cotyledon perfusion model consisting of seven compartments that can be used to mechanistically investigate placental drug transfer. The structure of this model is congruent with that of the placental compartments in the maternal-fetal PBPK model which allows a direct transfer of parameters from the former in the latter model. While the time of delivery will determine the time of collection of paired samples, at least the maternal part of a study protocol can be informed by predictions based on PK models, including PBPK models. The simulated accumulation of acetaminophen in the trophoblasts of the presented model might be of concern as this could potentially affect prostaglandin synthesis and subsequently fetal exposure to prostaglandins. Yet, it should also be stressed again that the measured drug concentrations in the maternal and fetal reservoirs were only to a limited extent informative of accumulation in the trophoblasts, as indicated by the sensitivity analysis result. Further studies should investigate potential accumulation as well as placental metabolism of acetaminophen.

The developed in silico cotyledon perfusion model is freely shared on OSP GitHub (https://github.com/Open-Systems-Pharmacology) for further applications and/or refinements that were beyond the scope of this study. Importantly, due to the mechanistic nature of the developed models, predictions can, in principle, be scaled to earlier stages of pregnancy (at least to the early second trimester when the formation of the placental barrier is completed). As clinical data are difficult to obtain at earlier stages of pregnancy, PBPK modeling approaches may constitute a potentially powerful tool to evaluate and investigate placental drug transfer and ultimately improve pharmacotherapy in pregnant women.

Data Availability Statement

The datasets analyzed for this study are referenced in the article. Clinical data reported by Mehraban et al. (18) can be obtained from Nisha Lakhi (Tkxha2hpJiN4MDAwNDA7cnVtY3NpLm9y) upon reasonable request.

Author Contributions

PM, KA, and AD designed the research and wrote the manuscript. PM and AD performed the research. PM, BN, JA, KC, KA, NL, and AD analyzed the data. All authors contributed to the article and approved the submitted version.

Conflict of Interest

AD is an employee of Bayer AG and uses Open Systems Pharmacology software, tools, and models in his professional role.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Acknowledgments

The authors would like to thank Dr. Sigrid Conings for conducting and analyzing the ex vivo cotyledon perfusion experiments.

References

1. Mitchell AA, Gilboa SM, Werler MM, Kelley KE, Louik C, Hernandez-Diaz S, et al. Medication use during pregnancy, with particular focus on prescription drugs: 1976–2008. Am J Obstet Gynecol. (2011) 205:51.e1–8. doi: 10.1016/j.ajog.2011.02.029

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Engeland A, Bjørge T, Klungsøyr K, Hjellvik V, Skurtveit S, Furu K. Trends in prescription drug use during pregnancy and postpartum in Norway, 2005 to 2015. Pharmacoepidemiol Drug Saf. (2018) 27:995–1004. doi: 10.1002/pds.4577

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Chaphekar N, Caritis S, Venkataramanan R. Model-informed dose optimization in pregnancy. J Clin Pharmacol. (2020) 60:S63–76. doi: 10.1002/jcph.1777

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Codaccioni M, Bois F, Brochot C. Placental transfer of xenobiotics in pregnancy physiologically-based pharmacokinetic models: structure and data. Computational Toxicol. (2019) 12:100111. doi: 10.1016/j.comtox.2019.100111

CrossRef Full Text | Google Scholar

5. Zhang Z, Unadkat JD. Development of a novel maternal-fetal physiologically based pharmacokinetic model II: verification of the model for passive placental permeability drugs. Drug Metab Dispos. (2017) 45:939–46. doi: 10.1124/dmd.116.073957

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Atoyebi SA, Rajoli RK, Adejuyigbe E, Owen A, Bolaji O, Siccardi M, et al. Using mechanistic physiologically-based pharmacokinetic models to assess prenatal drug exposure: thalidomide versus efavirenz as case studies. Eur J Pharm Sci. (2019) 140:105068. doi: 10.1016/j.ejps.2019.105068

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Codaccioni M, Brochot C. Assessing the impacts on fetal dosimetry of the modelling of the placental transfers of xenobiotics in a pregnancy physiologically based pharmacokinetic model. Toxicol Appl Pharmacol. (2020) 409:115318. doi: 10.1016/j.taap.2020.115318

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Liu XI, Momper JD, Rakhmanina NY, Green DJ, Burckart GJ, Cressey TR, et al. Prediction of maternal and fetal pharmacokinetics of dolutegravir and raltegravir using physiologically based pharmacokinetic modeling. Clin Pharmacokinet. (2020) 59:1433–50. doi: 10.1007/s40262-020-00897-9

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Mendes MDS, Hirt D, Vinot C, Valade E, Lui G, Pressiat C, et al. Prediction of human fetal pharmacokinetics using ex vivo human placenta perfusion studies and physiologically based models. Br J Clin Pharmacol. (2016) 81:646–57. doi: 10.1111/bcp.12815

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Mendes MDS, Lui G, Zheng Y, Pressiat C, Hirt D, Valade E, et al. A physiologically-based pharmacokinetic model to predict human fetal exposure for a drug metabolized by several CYP450 pathways. Clin Pharmacokinet. (2017) 56:537–50. doi: 10.1007/s40262-016-0457-5

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Schalkwijk S, Buaben AO, Freriksen JJ, Colbers AP, Burger DM, Greupink R, et al. Prediction of fetal darunavir exposure by integrating human ex-vivo placental transfer and physiologically based pharmacokinetic modeling. Clin Pharmacokinet. (2018) 57:705–16. doi: 10.1007/s40262-017-0583-8

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Freriksen JJ, Schalkwijk S, Colbers AP, Abduljalil K, Russel FG, Burger DM, et al. Assessment of maternal and fetal dolutegravir exposure by integrating ex vivo placental perfusion data and physiologically-based pharmacokinetic modeling. Clin Pharmacol Ther. (2020) 107:1352–61. doi: 10.1002/cpt.1748

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Mian P, Allegaert K, Conings S, Annaert P, Tibboel D, Pfister M, et al. Integration of placental transfer in a fetal-maternal physiologically based pharmacokinetic model to characterize acetaminophen exposure and metabolic clearance in the fetus. Clin Pharmacokinet. (2020) 59:911–25. doi: 10.1007/s40262-020-00861-7

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Liu XI, Momper JD, Rakhmanina N, van den Anker JN, Green DJ, Burckart GJ, et al. Physiologically based pharmacokinetic models to predict maternal pharmacokinetics and fetal exposure to emtricitabine and acyclovir. J Clin Pharmacol. (2020) 60:240–55. doi: 10.1002/jcph.1515

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Szeto KX, Le Merdy M, Dupont B, Bolger MB, Lukacova V. PBPK modeling approach to predict the behavior of drugs cleared by kidney in pregnant subjects and fetus. AAPS J. (2021) 23:89. doi: 10.1208/s12248-021-00603-y

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Tetro N, Moushaev S, Rubinchik-Stern M, Eyal S. The placental barrier: the gate and the fate in drug distribution. Pharm Res. (2018) 35:1–16. doi: 10.1007/s11095-017-2286-0

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Nitsche JF, Patil AS, Langman LJ, Penn HJ, Derleth D, Watson WJ, et al. Transplacental passage of acetaminophen in term pregnancy. Am J Perinatol. (2017) 34:541–3. doi: 10.1055/s-0036-1593845

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Mehraban S, Nematian S, Mehraban SS, Petrucci S, Tricorico G, Parnas Z, et al. Randomized control trial of intravenous acetaminophen for reduction of intrapartum maternal fever. Am J Obstet Gynecol MFM. (2021) 3:1–9. doi: 10.1016/j.ajogmf.2020.100287

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Mian P, Van Den Anker JN, van Calsteren K, Annaert P, Tibboel D, Pfister M, et al. Physiologically based pharmacokinetic modeling to characterize acetaminophen pharmacokinetics and N-acetyl-p-benzoquinone imine (NAPQI) formation in non-pregnant and pregnant women. Clin Pharmacokinet. (2020) 59:97–110. doi: 10.1007/s40262-019-00799-5

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Conings S, Tseke F, Van den Broeck A, Qi B, Paulus J, Amant F, et al. Transplacental transport of paracetamol and its phase II metabolites using the ex vivo placenta perfusion model. Toxicol Appl Pharmacol. (2019) 370:14–23. doi: 10.1016/j.taap.2019.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Lippert J, Burghaus R, Edginton A, Frechen S, Karlsson M, Kovar A, et al. Open systems pharmacology community—an open access, open source, open science approach to modeling and simulation in pharmaceutical sciences. CPT Pharmacometrics Syst Pharmacol. (2019) 8:878–82. doi: 10.1002/psp4.12473

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Beaulac-Baillargeon L, Rocheleau S. Paracetamol pharmacokinetics during the first trimester of human pregnancy. Eur J Clin Pharmacol. (1994) 46:451–4. doi: 10.1007/BF00191910

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Allegaert K, Peeters MY, Beleyn B, Smits A, Kulo A, Van Calsteren K, et al. Paracetamol pharmacokinetics and metabolism in young women. BMC Anesthesiol. (2015) 15:1–11. doi: 10.1186/s12871-015-0144-3

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Dallmann A, Ince I, Solodenko J, Meyer M, Willmann S, Eissing T, et al. Physiologically based pharmacokinetic modeling of renally cleared drugs in pregnant women. Clin Pharmacokinet. (2017) 56:1525–41. doi: 10.1007/s40262-017-0538-0

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Shintaku K, Arima Y, Dan Y, Takeda T, Kogushi K, Tsujimoto M, et al. Kinetic analysis of the transport of salicylic acid, a nonsteroidal anti-inflammatory drug, across human placenta. Drug Metab Dispos. (2007) 35:772–8. doi: 10.1124/dmd.106.013029

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Schmitt W. General approach for the calculation of tissue to plasma partition coefficients. Toxicol In Vitro. (2008) 22:457–67. doi: 10.1016/j.tiv.2007.09.010

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Dallmann A, Ince I, Meyer M, Willmann S, Eissing T, Hempel G. Gestation-specific changes in the anatomy and physiology of healthy pregnant women: an extended repository of model parameters for physiologically based pharmacokinetic modeling in pregnancy. Clin Pharmacokinet. (2017) 56:1303–30. doi: 10.1007/s40262-017-0539-z

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Valentin J. Basic anatomical and physiological data for use in radiological protection: reference values: ICRP publication 89: approved by the commission in September 2001. Ann ICRP. (2002) 32:1–277. doi: 10.1016/S0146-6453(03)00002-2

CrossRef Full Text | Google Scholar

29. Open Systems Pharmacology. Manual: Compounds: Definition and Work Flows. Available online at: https://docs.open-systems-pharmacology.org/working-with-pk-sim/pk-sim-documentation/pk-sim-compounds-definition-and-work-flow#distribution (accessed on March 4, 2021).

30. Rodgers T, Leahy D, Rowland M. Physiologically based pharmacokinetic modeling 1: predicting the tissue distribution of moderate-to-strong bases. J Pharm Sci. (2005) 94:1259–76. doi: 10.1002/jps.20322

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Rodgers T, Rowland M. Physiologically based pharmacokinetic modelling 2: predicting the tissue distribution of acids, very weak bases, neutrals and zwitterions. J Pharm Sci. (2006) 95:1238–57. doi: 10.1002/jps.20502

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Poulin P, Theil FP. A priori prediction of tissue: plasma partition coefficients of drugs to facilitate the use of physiologically-based pharmacokinetic models in drug discovery. J Pharm Sci. (2000) 89:16–35. doi: 10.1002/(SICI)1520-6017(200001)89:1<16::AID-JPS3>3.0.CO;2-E

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Poulin P, Schoenlein K, Theil FP. Prediction of adipose tissue: plasma partition coefficients for structurally unrelated drugs. J Pharm Sci. (2001) 90:436–47. doi: 10.1002/1520-6017(200104)90:4<436::aid-jps1002>3.0.co;2-p

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Polin RA, Fox WW, Abman SH. Fetal and Neonatal Physiology. Amsterdam: Elsevier health sciences (2011).

Google Scholar

35. Moniz C, Nicolaides K, Bamforth F, Rodeck C. Normal reference ranges for biochemical substances relating to renal, hepatic, and bone function in fetal and maternal plasma throughout pregnancy. J Clin Pathol. (1985) 38:468–72. doi: 10.1136/jcp.38.4.468

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Bouazza N, Foissac F, Hirt D, Urien S, Benaboud S, Lui G, et al. Methodological approaches to evaluate fetal drug exposure. Curr Pharm Des. (2019) 25:496–504. doi: 10.2174/1381612825666190319102812

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Noergaard M, Jensen PB, Gotfredsen DR, Bergholt T, Andersen JT, Mathiesen L. Therapeutic concentration of ciprofloxacin and transfer across the human term placenta. Am J Obstet Gynecol. (2021). doi: 10.1016/j.ajog.2021.05.032. [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Russo FM, Conings S, Allegaert K, Van Mieghem T, Toelen J, Van Calsteren K, et al. Sildenafil crosses the placenta at therapeutic levels in a dually perfused human cotyledon model. Am J Obstet Gynecol. (2018) 219:619.e1–10. doi: 10.1016/j.ajog.2018.08.041

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Freriksen JJ, Feyaerts D, van den Broek PH, van der Heijden O, van Drongelen J, van Hamersvelt H, et al. Placental disposition of the immunosuppressive drug tacrolimus in renal transplant recipients and in ex vivo perfused placental tissue. Eur J Pharm Sci. (2018) 119:244–8. doi: 10.1016/j.ejps.2018.04.017

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Syme MR, Paxton JW, Keelan JA. Drug transfer and metabolism by the human placenta. Clin Pharmacokinet. (2004) 43:487–514. doi: 10.2165/00003088-200443080-00001

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Myllynen P, Immonen E, Kummu M, Vähäkangas K. Developmental expression of drug metabolizing enzymes and transporter proteins in human placenta and fetal tissues. Expert Opin Drug Metab Toxicol. (2009) 5:1483–99. doi: 10.1517/17425250903304049

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Stanley EL, Hume R, Visser TJ, Coughtrie MW. Differential expression of sulfotransferase enzymes involved in thyroid hormone metabolism during human placental development. J Clin Endocrinol Metab. (2001) 86:5944–55. doi: 10.1210/jcem.86.12.8081

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Allegaert K, Mian P, Lapillonne A, van den Anker JN. Maternal paracetamol intake and fetal ductus arteriosus constriction or closure: a case series analysis. Br J Clin Pharmacol. (2019) 85:245–51. doi: 10.1111/bcp.13778

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Allegaert K, van den Anker JN editors. Perinatal and Neonatal Use of Paracetamol for Pain Relief. Seminars in Fetal and Neonatal Medicine. Amsterdam: Elsevier (2017).

PubMed Abstract | Google Scholar

45. van den Anker J, Allegaert K. Acetaminophen use in pregnant women and their neonates: safe or unsafe till proven otherwise? Neonatol Fetal Neonatal Res. (2020) 117:249–51. doi: 10.1159/000506837

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Saugstad OD. Acetaminophen and the developing brain: reason for concern? Neonatology. (2020) 117:245–8. doi: 10.1159/000505954

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Granger JP, Alexander BT, Bennett WA, Khalil RA. Pathophysiology of pregnancy-induced hypertension. Am J Hypertens. (2001) 14:178S−85. doi: 10.1016/S0895-7061(01)02086-6

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Nylund L, Lunell N-O, Lewander R, Persson B, Sarby B. Uteroplacental blood flow in diabetic pregnancy: measurements with indium 113m and a computer-linked gamma camera. Am J Obstet Gynecol. (1982) 144:298–302. doi: 10.1016/0002-9378(82)90582-8

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Mazzanti L, Staffolani R, Rabini R, Romanini C, Cugini A, Benedetti G, et al. Modifications induced by gestational diabetes mellitus on cellular membrane properties. Scand J Clin Lab Invest. (1991) 51:405–10. doi: 10.3109/00365519109091633

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Al-Okail MS, Al-Attas OS. Histological changes in placental syncytiotrophoblasts of poorly controlled gestational diabetic patients. Endocr J. (1994) 41:355–60. doi: 10.1507/endocrj.41.355

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Meng Q, Shao L, Luo X, Mu Y, Xu W, Gao C, et al. Ultrastructure of placenta of gravidas with gestational diabetes mellitus. Obstet Gynecol Int. (2015) 2015:283124. doi: 10.1155/2015/283124

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: acetaminophen, ex vivo cotyledon perfusion, physiologically-based pharmacokinetics, placental transfer, maternal-fetal, pregnancy

Citation: Mian P, Nolan B, van den Anker JN, van Calsteren K, Allegaert K, Lakhi N and Dallmann A (2021) Mechanistic Coupling of a Novel in silico Cotyledon Perfusion Model and a Physiologically Based Pharmacokinetic Model to Predict Fetal Acetaminophen Pharmacokinetics at Delivery. Front. Pediatr. 9:733520. doi: 10.3389/fped.2021.733520

Received: 30 June 2021; Accepted: 20 August 2021;
Published: 23 September 2021.

Edited by:

Venkata Kashyap Yellepeddi, The University of Utah, United States

Reviewed by:

Alexandre Bonnin, University of Southern California, United States
Vijay K. Siripuram, University of Florida, United States

Copyright © 2021 Mian, Nolan, van den Anker, van Calsteren, Allegaert, Lakhi and Dallmann. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Paola Mian, UGFvbGEuTWlhbiYjeDAwMDQwO21zdC5ubA== orcid.org/0000-0002-3551-1201

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