The thermal decomposition method is the most facile to create high-quality Ln-UCNPs. Thermal decomposition is the process of pyrolyzing organometallic precursors in an organic solvent under an oxygen-free environment. In general, the precursors are organic salts of rare Earth ions, such as trifluoroacetate and acetate among others. Octadecene (ODE) is the most frequently used high-boiling organic solvent. Oleic acid (OA) and oleylamine (OM) can serve dual roles as solvents and as ligands that adsorbed onto the nanoparticles to control their size and shape. It is worth noting that the crystal nucleation and growth process that control the nanoparticle uniformity can be adjusted with the temperature, heating rate, and precursor concentrations during synthesis.

Yan and co-authors first synthesized LaF₃ crystals by thermal decomposition using a single-source precursor (Zhang et al., 2005). Later they pioneered the use of multi-source precursors to prepare high quality nanocrystals through thermal decomposition, which greatly promoted the development of Ln-UCNPs (Yin et al., 2010). Murray and collaborators studied the influence of reaction time and the ratio of sodium to lanthanide precursors on the morphology of β-NaYF₄-based Ln-UCNPs in detail, thereby obtaining beautiful rare earth-based nanocrystals (Ye et al., 2010). We applied LnCl₃ (Ln = Y and Er) as precursors in an OA and ODE mixture that was heated to a high temperature, next NH4F and NaOH were added to obtain core nanoparticles of NaYF₄:Er. Finally Lu(CF₃COO)₃ and CF₃COONa mixed with NaYF₄: Er were further processed under high temperature and oxygen-free environment to obtain stable NaYF₄:x%Er@NaLuF4 (Feng et al., 2018).

Ln-UCNPs synthesized using the thermal decomposition method are highly monodisperse and uniform in shape. They also display greater up-conversion emission intensity; however, the syntheses are complicated and the products are lipophilic and not stable, which limits the application of thermal decomposition in Ln-UCNPs synthesis.

The hydrothermal/solvothermal method is facile for synthesizing Ln-UCNPs under mild conditions at a low cost. Generally, hydrothermal syntheses are carried out in a reactor to provide a high-pressure environment. Simple rare Earth nitrates or chlorides are used as precursors for the preparation of Ln-UCNPs. The most common solvents are water, ethanol, glycol and other simple hydrophilic inorganic/organic solvents (Rafique et al., 2019). Li and co-workers introduced oleic acid into solvothermal synthesis. As an oleophilic organic solvent, it broadened the range of materials and structures that can be realized using this method (Wang et al., 2005). The selection of organic additives has a significant impact on the morphology and size of the product. Hydrophilic organic ligands that can adhere to the surface of products and inhibit particle aggregation can endow the nanocrystals with good hydrophilicity, biocompatibility, and functionalizability with biomolecules. It was reported that ethylene diamine tetra acetic acid (EDTA), polyvinyl pyrrolidone (PVP), hexadecyl trimethyl ammonium bromide (CTAB) and polyacrylic acid (PAA)/poly ethylenimine (PEI) as additives improve the morphology and dispersion of Ln-UCNPs (Mousavand et al., 2010; Li et al., 2020a). A mixed solution of Ln(NO₃)₃, Y:Yb:Tm = 70:30:0.5, was used as a rare Earth precursor with EDTA as an organic additive. NaYF₄: Yb³⁺, Tm³⁺ were synthesized by high temperature and pressure in a reactor (Xu et al., 2020). The advantages of hydrothermal/solvothermal method include the potential for large-scale production. Moreover, the reaction is always carried out under closed conditions without harmful gas leakage, so it is environmentally friendly and non-toxic. However, these conditions also make it impossible to observe the crystal growth process, which impede the studies into the reaction mechanisms.

The products of the co-precipitation method are usually chemically homogeneous and uniformly distributed; however, the surfaces are rough and difficult to control. Coudret et al. obtained ultra-small Na(Gd-Yb)F₄:Tm through an improved co-precipitation method (Figure 1). In addition to the synthesis of specific precursors and microwave-assisted heating, the influence of oleic acid content on heating efficiency was discussed (Amouroux et al., 2019). In 2014, Liu and co-workers demonstrated a simpler co-precipitation method to prepare core-shell NaGdF4 nanoparticles doped with luminescent lanthanide ions that did not require precise control of the feeding rate of shell precursors. However, the large core-shell nanocrystals had a low up-conversion efficiency (Wang et al., 2014b). Jin and co-workers synthesized a near-infrared (NIR) fluorescence “turn-on” kit based on rare Earth ion-doped nanoparticles and gold nanoparticles, which created an HIV-1 based DNA detection system that was simple, homogeneous, and highly selective (Zhou et al., 2019). Chen and co-workers were the first to report the synthesis of CaS:Eu²⁺,Sm³⁺ near infrared photostimulated luminescence nanocrystals by a high temperature co-precipitation method. The materials exhibited a fast response to stimuli over 800–1,600 nm (Gao et al., 2019). In conclusion, the application of the co-precipitation method creates products that have biomedical applications; however, they are limited by defects. Regardless, this simple process is conducive to industrial production.

In addition to the processes discussed previously, several novel methods have been developed for the synthesis of Ln-UCNPs. For instance, microemulsions and ionic liquids have been applied, and Ln-UCNPs have been prepared using microwave heating. The microemulsion method creates materials in droplets that contains the surfactant, cosurfactant, solvent and water. Few product nanoparticles are prepared this way; furthermore, the dispersion is poor because the growth of the particles is affected by the size of the micelle. Li and colleagues reported a method of microemulsion assisted synthesis of functionalized Ln-UCNPs. The nanoparticles was synthesized in a heterogeneous oil-water microemulsion phase, and the product had a high cross-section and adjustable pore size (Dai et al., 2020).

Microwave synthesis has unique properties, including increased speed and heating efficiency, which contributes to energy savings and environmental protection. It was reported that NaGdF₄:Yb, Er can be directly synthesized using a microwave digestion/extraction system; furthermore, the produced have good biomedical application prospects (Li et al., 2012).

Up-conversion is the process of converting low-energy photons into high-energy luminescence, which relies on energy transfer within the 4f electron manifold of the luminescent ions. Luminescence mechanisms include excited state absorption (ESA), energy transfer up-conversion (ETU), and cooperative sensitization up-conversion (CSU). The ESA process occurs within a single ion that continuously absorbs photons to create upconverted luminescence. The ETU process involved in a pair of neighboring rare Earth ions, a sensitizer as energy donor, and an activator as energy acceptor. After excitation, the ground state sensitizer ion becomes electronically excited, the energy from which is transmitted to activators. In turn the activator ion transitions to a higher electronic state, and then luminesces to the ground state. The CSU process requires at least three ion centers. Two of them are the same element that act as sensitizers. They can interact with activators simultaneously in the excited state, which in turn transfers energy to activators. Consequently, the doping of rare Earth ions is closely related to the up-conversion luminescence ability of the nanoparticles, and the luminescence intensity can be regulated by adjusting the species and concentration of rare Earth ions.

Ln-UCNPs are composed of activators and sensitizers within a matrix. For up-conversion, the matrix must have excellent optical properties and stability. The most studied are fluoride materials NaYF₄, LaF₃, LiYF₄, and NaGdF₄ among others (Wang et al., 2011; Liu et al., 2012; Wang et al., 2014b; Zhang et al., 2015). To achieve up-conversion luminescence, the energy difference between at least three adjacent energy levels of the activator should be in close proximity. Therefore, Er³⁺, Tm³⁺ and Ho³⁺ are the most important due to their step-like energy levels. Sensitizer ions are usually introduced due to the fact that the luminous efficiency of single-doped Ln-UCNPs is not high. Yb³⁺ has become the most common sensitizer due to its unique energy level structure (Han et al., 2014).

We synthesized highly doped Er³⁺ core-shell nanoparticles of NaYF₄:x%Er@NaXF₄ (x = 5, 25, 50, and 100; X = Lu and Y). The effect on luminescence as a function of Er³⁺ concentration was studied. There was a significant enhancement of red emission at 100% Er³⁺ doping (Feng et al., 2018). In a sensitizer and activator co-doped system, the concentration of activator generally does not exceed 5% while the sensitizer concentration is relatively high, on the order of 15%–40%. The emission of Yb³⁺/Er³⁺ co-doped systems range from 510 nm to 560 nm (green) and 640 nm–670 nm (red). This system can emit with multiple colors as a combination of green and red can produce yellow light. Er³⁺/Yb³⁺ co-doped Na_0.5Gd_0.5Mo_O4 was reported to emit with characteristic peaks at 531/552/667 nm; furthermore, the intensity of UCL increased with higher Yb³⁺ concentration over a certain range (Du et al., 2016). Similarly, the intense emission of the Yb³⁺/Tm³⁺ co-doped system was in the blue region, while the Yb³⁺/Ho³⁺ co-doped system mostly emitted green light with improved efficiency due to the sensitizer. Rare Earth ions have further utility. For example, multi-doped systems empower enhanced luminescence modulation. Liu et al. reported white light emission from Er³⁺/Tm³⁺/Yb³⁺ triple-doped SrLu2O4. The Yb³⁺ concentration and pump power can be tuned to modulate the emission color. The optimal doping ratio of 0.5% Er³⁺, 0.5% Tm³⁺, and 20% Yb³⁺ created the best balance of red, green and blue luminescence to produce bright white light emission (Liu et al., 2018a). Dammak and coworkers designed a white light modulation system, Yb³⁺/Er³⁺/Tm³⁺ doped GdPO₄ at a high concentration of Yb³⁺ (35%mol), which emitted white light with excitation by an appropriate laser power (Hassairi et al., 2018). β-NaYF₄: Yb³⁺, Ho³⁺, Tm³⁺ triple-doped Ln-UCNPs can create multicolor UCL by adjusting the doping concentration and excitation power, which resulted in both white and red light output (Gao et al., 2017).

Metal nanoparticles exhibit a strong plasmon resonance intensity due to electron delocalization over a large surface area. The surface plasmon resonance (SPR) effect will occur when the frequency of the incident photon is the same as the surface plasma oscillation. At this time, a strong local electric field is generated around the metal nanostructure, which further increases the excitation and radiation decay rates of Ln-UCNPs and thus enhances the up-conversion luminescence. UCL can be enhanced by SPR (Thariani and Yager, 2010), which prompted us to theoretically explore the effects of metal nanoparticles on Ln-UCNPs luminescence using the Discrete Dipole Approximation (DDA). The DDA algorithm can calculate the electromagnetic properties of nanoparticles as a function of shape. We synthesized La2O3:Yb/Er@Au, the gold coating of which significantly enhanced the emission intensity of La₂O₃:Yb/Er@Au by 16.8 times. Experiments demonstrated that the amount of Au added affects the particle spacing and the intensity of UCL. The increase in the electric field simulated by DDA was in good agreement with the observations made in the presence of an Au coating (Lv et al., 2014a). Light exposure and heating of the metal were shown to result in drug release in Na₅Lu₉F₃₂:Yb/Er@Au. Both DDA simulation and experimental studies of Ln-UCNPs revealed that the coating of Au enhanced the absorptivity, which in turn resulted in a temperature increase upon excitation that facilitated the release of doxorubicin (DOX). Therefore, this system can be used for controlled drug release by the photothermal effect (Lv et al., 2014b). In the first two systems, we only performed electromagnetic calculations on single Au nanoparticles. DDA was used for the first time to perform extinction calculations on the rare earth-metal model of Ln-UCNPs@SiO₂-Au (Figure 2A) (Lv et al., 2018a). The results revealed the potential to use DDA to guide the construction of rare earth-metal composite materials.

Although considerable progress has been made, many issues remain to be addressed. In the simulations discussed above, gold shells were used to simulate gold coatings. To obtain more accurate results, the Au shells were replaced with randomly distributed gold spheres to simulate Ln-UCNPs@mSiO₂-Au. Both DDA simulation and experiments demonstrated that the presence of 5 nm Au spheres results in enhancements; however the experimental results on 20 nm Au sphere were inconsistent with the DDA simulations due to insufficient uniformity and aggregation. Regardless, the overall accuracy of the model on the modulation of the luminescence was improved (Lv et al., 2020). Next, we synthesized Au/Ag@Ln-UCNPs, and used DDA to simulate the enhancement on UCL due to the presence of gold nanocages of different sizes and thicknesses. Optical characterizations revealed that the luminous intensity of Au/Ag@Ln-UCNPs is twice that of Ln-UCNPs alone. In addition, Au/Ag@Ln-UCNPs were also effective for PTT/PDT treatment of tumors (Liu et al., 2019b). Additionally, Ln-UCNPs@SiO₂@Au (SPS@Au) was synthesized and coated with ZnPc (zinc phthalocyanine) to produce SPS@Au/ZnPc. DDA was used to simulate the extinction of SPS@Au/ZnPc as a function of gold particle content (Figure 2B), the results from which revealed enhanced luminescence properties (Lin et al., 2020).

The finite difference time domain (FDTD) method can be used to simulate the enhancement of UCL due to metal SPR. Song and coworkers used FDTD to simulate NaYF₄: Yb³⁺, Er³⁺ up-conversion luminescence in the presence of a gold rod. Single-layer gold nanorod (GNRs) and Ln-UCNPs were assembled on both sides of an isolating MoO₃ layer to demonstrate a luminescence enhancement effect of more than 35 times (Yin et al., 2016). Zhou and coworkers used FDTD to model Ag@SiO₂ to calculate the optimal Ag particle size and silicon layer thickness. The prepared Ag@SiO₂@YF₃:Ho³⁺ nanoparticles exhibited better luminous intensity (Xu et al., 2019). Although enhancements are realized using the current strategy of metal modulation to enhance UCL, the effects are actually quite modest. Methods to achieve greater optical enhancements is a problem to be solved in the future.

A large number of experiments are usually required to determine the optimal doping concentration for Ln-UCNPs.

However, computer technology has revolutionized the traditional screening method. Using algorithms to guide this process can greatly simplify experimental realization. The doping optimization of rare Earth luminescent powder is essentially a combination optimization problem. A product can be designed on a computer and then experimentally realized; these steps are repeated to obtain a material with the best properties. In this process, heuristic algorithms based on natural body algorithms, have been used to guide the synthesis of rare earth-doped luminescent powders with high quantum yield. Heuristic algorithms include the genetic algorithm (GA), particle swarm optimization (PSO), and simulated annealing (SA) (Hopper and Turton, 2001; Hamza et al., 2017; Ozdemir and Karaboga, 2019). GA is a global random search optimization algorithm that uses the “survival of the fittest” mechanism to derive relationships between the material properties and the mole percentage of each raw material, and is often used to guide chemical synthesis optimization problems (Katoch et al., 2021). PSO simulates “bird predation.” The algorithm is easy to understand and program, has global search ability; as a result it has been applied in the field of combinatorial chemistry. Annealing is the process in which the temperature of the system decreases with time (Thangaraj et al., 2011). SA continuously iterates a simulated annealing process to find a solution that meets design specifications (Suman and Kumar, 2006). This algorithm has not yet been applied to combinatorial chemistry problems. Therefore, the most widely used optimization algorithm is the genetic algorithm (Lv et al., 2018b).

Our group has studied the pros and cons of SA, the improved SA of harmony search, PSO, and GA for guiding the synthesis of luminescent powders (Figure 3). The efficacy of the four algorithms were evaluated by taking the same first-generation luminescent powder as the starting point for optimization and performing 5 iterations. SA had no obvious optimization effect; however, better results were obtained when combined with the harmony search. The genetic algorithm was better than PSO; however, generational analysis found that the brightness of the luminous powders as guided by PSO was more gradual (Lv et al., 2019).

In recent years, it was reported that the regression equation was built through the experimental results, which showed the relationship between luminescence and doping concentration. Then genetic algorithm was used to get the doping concentration corresponding to the maximum luminescence intensity (Sun et al., 2015). Coincidentally, Zhao et al. (2019) used the genetic algorithm to modulate Er³⁺/Yb³⁺ co-doped Ba5Gd8Zn4O21, resulting in efficient red light emission.

Ln-UCNPs are challenged with weak absorptions and narrow optical excitation regions. These issues can be addressed using the dye sensitization strategy in which organic near-infrared chromophores are coordinated to the surface of Ln-UCNPs. Examples include IR783, IR806, IR808, and indocyanine green (ICG) which act as “antennas” to capture photons and transfer energy to the up-conversion rare Earth particles to improve UCL (Hazra et al., 2018). In 2012, Zou et al. (2012) used IR806 to sensitize β-NaYF₄: Yb, Er for the first time. In this study, the intensity of up-conversion luminescence via excitation with an 800 nm laser increased by 1,100 times compared to that realized from excitation at 980 nm. This work prompted widespread application of this strategy for up-conversion luminescence enhancement. Han and coworkers synthesized (β-NaYF₄: 20% Yb³⁺, 2% Er³⁺) Ln-UCNPs without hydrophobic organic ligands, and then explored the best ratio of near-infrared dyes to Ln-UCNPs to enhance luminescence. They coordinated IR783, IR808, IR820 and IR845 to Ln-UCNPs, and found enhancements of 80, 200, 70 and 10, respectively. To explore the sensitization effect of multiple dyes, IR783 and IR845 were simultaneously coordinated to the same Ln-UCNPs. The multidye-sensitized Ln-UCNPs showed a wider wavelength range and were applied for orthogonal bioimaging (Wu et al., 2015). Chen et al. proposed a new concept of energy-cascaded up-conversion (ECU) through the design of an IR808-sensitized core/shell Ln-UCNPs. IR808 was coordinated to the Ln-UCNPs and acted as an antenna to collect excitation energy that was transferred to Nd³⁺, Tm³⁺ and Yb³⁺ through a multi-step process. This approach achieved a high up-conversion quantum efficiency of 19% (Chen et al., 2015).

Although the sensitization strategy can significantly enhance UCL, the dyes are quenched in water which greatly limits potential applications. Researchers have explored the synthesis of more stable and brighter dye-sensitized Ln-UCNPs. It was reported that Ln-UCNPs sensitized with Cy7 enhanced UCL in ethanol by ∼30 times, although the effect was limited in water by ∼2 times. To address this problem phosphatidylcholine was introduced to improve water dispersibility, which resulted in an increase of 17 times efficiency and enabled lymphatic imaging (Zou et al., 2016). Liu and coworkers revealed that quenching of dye sensitized Ln-UCNPs in water is the result of dye aggregation. Generally, near-infrared dyes are coupled to Ln-UCNPs through chemical coordination; in contrast, Liu and coworkers constructed dye-sensitized systems through hydrophobic interactions. The amphiphilic molecule DSPE-PEG (1,2-distearoyl-n-glycerol-3-phosphoethanolamine-N- [(polyethyleneglycol)-methoxy]) was used to coat the dye Car-Cl. As a result, the sensitization was improved 85 times in water. Unfortunately, aggregation-induced quenching was nonetheless observed at high concentrations.

To further eliminate strong coordination between the dye and rare Earth ions, Liu and coworkers used two long hydrophobic alkyl chains to replace the carboxyl group of the dye Car-Cl to produce a new dye (Alk-Cl), the use of which achieved enhancement of UCL of 215 times (Figure 4) (Liang et al., 2020a). In addition, NIR-II dye (IR-1061) was used to sensitize core-shell Ln-UCNPs and solve the problem of quenching in water. It was worth noting that the purpose of this research was not to enhance up-conversion, rather, to obtain a strong near-infrared signal. Application of this strategy resulted in an increase in the 800 nm emission of Tm³⁺ ions by 2.83 times. Furthermore, the near-infrared emission had a deeper tissue penetration depth, which is more conducive for biological imaging compared to visible emitters (Hazra et al., 2018). Although Ln-UCNPs have multicolor emission, it should be noted that red light has the advantages of deep penetration depth and imparts minimal damage to tissues in biological application.

During the synthesis of nanoparticles, long-chain polymers like oleic acid always were wrapped on the surface of Ln-UCNPs. In this way, the stability and luminescence intensity in aqueous are decreased compared with organic solvents, which limits the application in organisms. The following methods are usually used to deal with synthesized Ln-UCNPs. 1) Acid or excess ethanol was added. The ligands on the surface of Ln-UCNPs can be removed under the ultrasound. Capobianco and co-workers successfully removed the oleic acid ligands on the surface of NaGdF₄: Yb³⁺,Er³⁺ by the means of acid treatment (Bogdan et al., 2011) 2). The hydrophobic ligands were replaced by hydrophilic ligands, such as PEI, PAMAM, and PAA, to increase the water solubility of the nanoparticles. (Kovalenko et al., 2009; Kovalenko et al., 2010; Tangirala et al., 2010) 3) Inorganic material shells were coated on the surface of Ln-UCNPs, such as SiO_2. This method can improve the water solubility of the nanoparticles effectively. It is worth noting that, thickness of the SiO₂ needs to be determined by multiple experiments. Since too thick or too thin SiO₂ layers may affect the luminescence intensity of Ln-UCNPs and make the synthesis process more difficult. (Li and Zhang, 2006)

Drug delivery is an important part of cancer treatment. Generally, Ln-UCNPs can be used as a vehicle for drug delivery to achieve a specific therapy. Mechanisms for drug delivery using Ln-UCNPs include passive, active, and physical targeting. In the passive targeting strategy, drugs are combined with Ln-UCNPs to achieve targeted therapy with the help of the enhanced permeability and retention (EPR) effect. In the active targeting strategy, drugs are combined with Ln-UCNPs, and the interaction between a ligand and receptor, or antigen and antibody, is used to specifically recognize cells to achieve the targeted delivery of drugs. Chen et al. (2017) designed Tm³⁺-doped UCNPs and combined them with light-activated Ru complexes, so that enzyme inhibitors can be released by NIR excitation. In the physical targeting strategy, designer nanoparticles can be used to release drugs in specific locations by external environmental stimulus, such as changes in pH or temperature, photoexcitation, or magnetic targeting. Lin and coworkers designed Ln-UCNPs doped with Yb³⁺ and Tm³⁺ with additional modification of hydrazine monohydrate on the surface. In an acidic environment, the hydrogen bonds in the nanoparticles dissociate, enabling drug release (Yang et al., 2014). Mykhaylyk et al. (2001) designed magnetic nanoparticles that can deliver drugs to penetrate the blood-brain barrier and enter the mouse brain (Mykhaylyk et al., 2001). De et al. designed a polyelectrolyte complex based on Yb³⁺ and Er³⁺ to deliver pharmaceutical grade protein (De et al., 2022). The modified nanosystem overcame the problem of protein aggregation in the cell membrane and protected the protein drugs from destruction by proteases and the action of heat. At the same time, the nanoscale drug carrier system responded to the 980-nm NIR light, and realized the imaging of the protein delivery process.

PDT has been clinically applied as a supplement to traditional therapy. Porphyrin is the first photosensitizer approved for this purpose (Tian et al., 2020), and mTHPC (meso-tetra hydroxy phenyl chlorin), a second generation photosensitizer, has shown many excellent characteristics in photodynamic therapy (Pinto et al., 2021; Yakavets et al., 2021; Yuan et al., 2021). In addition, chlorin dihydrogen E6 (Chlorin e6, Ce6), ZnPc and other photosensitizers have been widely used in scientific research although they have not been clinically approved (Chen et al., 2021a; Zhang et al., 2021a; Chen et al., 2021b; Hu et al., 2021; Lee et al., 2021; Shen et al., 2021; Zheng et al., 2021). Most photosensitizers are hydrophobic and easily aggregate in solution, which introduces practical difficulties (Liu et al., 2021a; Lin et al., 2021; Wei et al., 2021; Wu et al., 2021). Compared with PDT, there are less examples of the clinical application of PTT for tumor treatment. ICG is a dye that has been widely used in clinical diagnosis (Lutken et al., 2021; Teng et al., 2021). It can absorb in the near-infrared (600–900 nm) which enhances tissue penetration. In addition to its use in imaging and diagnosis, ICG has high photothermal conversion efficiency for photothermal therapy which is helpful for follow-up treatment of tumors (Ravichandran et al., 2020; Zhang et al., 2021b).

Currently, most of the photothermal agents are still applied in preclinical or early clinical research due to the fact that photothermal reaction cannot not completely eradicate a tumor; furthermore, there are additional risks due to overheating caused by laser ablation (Gao et al., 2020; Guo et al., 2021; Li et al., 2021; Pang et al., 2021; Zhao et al., 2021).

Ln-UCNPs are candidates for phototherapy due to their low toxicity and ability to be excited by near-infrared light. Ln-UCNPs are often used to deliver other molecules or add modifiers, for which the ability to upconvert expands the range of usable therapeutic agents making it more suitable for cancer phototherapy. In most cases, PDT and PTT effects exist simultaneously (Yang et al., 2021a; Bian et al., 2021; Yang et al., 2021b).

Generally, Ln-UCNPs is used in phototherapy to convert near infrared into visible light to trigger a photodynamic response. Guang and co-workers synthesized BiNS@NaLnF₄(Ln = Gd) using a solvothermal method (Figure 5A). Specifically, NaGdF4 was loaded onto Bi ultra-thin nanosheets, and up-conversion was observed under 980 nm laser irradiation to stimulate ROS generation. NaLnF₄ has a light-to-heat conversion efficiency of 35.3% (Ma et al., 2021a). Ln-UCNPs can also be used as a light energy converter to participate in the reconstruction of a tumor’s microenvironment (Figure 5B). The emitted light of a Ln-UCNPs can activate a photoacid to release H⁺, which reduced the pH value of the tumor environment and improved the release of ROS in the cell in response to acid environment (Wang et al., 2020). Liu et al. (2020) synthesized an injectable DNA-Ln-UCNPs-Au hydrogel, which enhanced the aggregation of Ln-UCNPs-Au through electrostatically complexed DNA strands and achieved a photothermal conversion efficiency of 42.7% (Figure 5C). In in vivo experiments, DNA-Ln-UCNPs-Au showed good stability and anti-cancer activity. In these preclinical studies, Ln-UCNPs have played an important role for tumor treatment. Since the excitation wavelength is in near-infrared band, phototherapy based on Ln-UCNPs can avoid the self-absorption problem of biological tissues and increase the penetration depth.

Chemotherapy can address the shortcomings of phototherapy, while phototherapy can more accurately target tumors and can be used to visually monitor drug release when combined with bioimaging (Andre et al., 2020; Birtle et al., 2020; Zheng and Xu, 2020; Yan et al., 2021b). A Ln-UCNPs-based multifunctional platform, Ln-UCNPs@PDA@Cy3-pep, that has treatment and real-time monitoring functions was reported (Liu et al., 2021b). The Ln-UCNPs comprised the core, while the chemotherapeutic drug staurosporine (STS) was loaded on the polydopamine (PDA) shell. The complex was shown to be effective for both photothermal therapy and chemotherapy under near infrared light irradiation. The quenching and restoration of Cy3 fluorescence was used to monitor the anti-cancer efficiency of the complex in real time (Liu et al., 2021b). Ju and coworkers reported a combination of chemical-photodynamic therapy based on a dual emitting Ln-UCNPs that was functionalized with a photosensitizer and the prodrug camptothecin. The surface was modified to enhance water solubility and targeting. Near-infrared excitation resulted in ultraviolet emission that activated the toxicity of CPT, and additional blue emission activated the photosensitizer to produce singlet oxygen to kill cancer cells (He et al., 2021). Huang and coworkers modified the photosensitizer to the surface of Ln-UCNPs to obtain Ln-UCNPs@PFNS. AQ4N, a hypoxia-activated prodrug that displays high toxicity selectively to hypoxic environment, was added to the pH-sensitive surface coating for chemotherapy (Figure 6). The surface coating decomposed at the tumor site due to the acidic environment, resulting in exposure of AQ4N and the photosensitizer. Under near-infrared excitation the photosensitizer generated ROS and aggravated the hypoxia at the tumor site which enhanced the therapeutic effect of hypoxia-activated AQ4N (Ji et al., 2019). It is promising to actively explore therapies that can assist chemotherapy given its role as the dominant cancer treatment. It is foreseeable that the structure and optical properties of Ln-UCNPs will add value in chemotherapeutic approaches to treat cancer more effectively (Liang et al., 2020b).

In recent years, immunotherapy has attracted attention due to the targeting capability and increased safety. Tumor immunotherapy does not reply on external stimuli, rather, it activates the immune response and cultivates immune cells to attack cancer cells (Tan et al., 2020a). Unlike traditional therapies, cancer cells can be removed continuously and quickly. Due to the efficacious anti-cancer effects of anti-CTLA-4 and anti-PD-1 antibodies, immunotherapy has the potential to revolutionize tumor treatment (Kamata-Sakurai et al., 2021; Tay et al., 2021). Many studies have demonstrated the potential for immunotherapy to improve the survival rate of patients and improving quality of life (Borcoman et al., 2019; Wallis et al., 2019; Mpekris et al., 2020). The combination of Ln-UCNPs-based phototherapy and immunotherapy may augment each other’s therapeutic effects. Liu et al. prepared a core-shell structure with a core PDA, a NaGdF₄:Yb/Er shell, and modified it with the photosensitizer Ce6 (Figure 7A). When irradiated with a 980 nm laser, the PDA component of the PDA@Ln-UCNPs-PEG/Ce6 acted as a photothermal agent while the Ce6 functioned as a photodynamic therapy agent. Phototherapy stimulated the body to produce an immune response, activated T lymphocytes and T memory cells, and helped to inhibit tumor metastasis and recurrence. However, it did not protect the mice from death threats caused by cancer. When combined with the immunosuppressant PD-1, the survival rate of mice was significantly improved to 77.8%, demonstrating the advantages of immunotherapy in long-term survival (Yan et al., 2019). Similarly, Chen and co-authors constructed a Ln-UCNPs/ICG/rose bengal (RB-mal) system (Figure 7B) that triggered enhanced phototherapy by ICG under near-infrared irradiation. Tumor-derived protein antigen was captured by the nano-platform and kept in place to trigger a systemic anti-tumor immune response. Experiments in mice proved that Ln-UCNPs/ICG/RB-mal can not only cure tumors in situ, but also inhibits the growth of distant tumors, illustrating the generation of a tumor-specific immune response (Wang et al., 2019a). In addition, Ln-UCNPs can stimulate the immune response. Li and co-workers combined Ln-UCNPs with PCpG for immunotherapy (Figure 7C). The core-shell nanoparticles NaGdF₄:70%Yb, 1%Tm@NaGdF₄ emitted at 313, 363, 453 and 478 nm under 980 nm laser excitation. The UV light activated PCpG to release the immunotherapy agent CpG. In mouse experiments, it was worth noting that the CpG/UCs conjugate proved more effective compared to PCpG/UCs + NIR; however, the former caused severe systemic toxicity which reveals the advantages of using Ln-UCNPs in this process (Chu et al., 2019).

When combining phototherapy with immunotherapy, both the near-infrared irradiation and phototherapy reagents elicit the body’s immune response (Hou et al., 2018; Dai et al., 2020; Sun et al., 2020). However, the process is not clear, and as such exploring complex systems that can cause an immune response is still an urgent issue to be solved.

Fluorescence imaging generally uses photoluminescence probes, for which Ln-UCNPs are excellent candidates as their application does not result in tissue damage (Hu et al., 2020; Zhang et al., 2020). Recently, Hao and co-workers synthesized polyacrylic acid-modified NaLnF4: 40Gd/20Yb/2Er, (Ln = Y, Yb, Lu, PAA-Ln-NRs). PAA-Ln-NRs with bright NIR II emission were injected into the tail vein of mice, and under excitation from a 980 nm laser they achieved high-precision imaging of small tumors and metastases that enabled early cancer diagnosis (Wu et al., 2019). Liu et al. synthesized dye-sensitized Ln-UCNPs with a reduced propensity for aggregation in water through hydrophobic coordination. Issues with the quenching of Ln-UCNPs luminescence in water was addressed by adjusting the dye absorption band (Liang et al., 2020a). Chen et al. designed an ingenious NaYF₄@NaYbF₄@NaYF₄:Yb³⁺/Tm³⁺@NaYF₄ structure for multi-channel fluorescence imaging. After intravenous and subcutaneous injection of the Ln-UCNPs, clear in vivo color imaging was obtained (Li et al., 2020b). The Fuyou group (Qiu et al., 2017; Liu et al., 2018b; Park et al., 2018) recently synthesized a rare-earth probe with NIR-II imaging capability. Ce³⁺ doping significantly increased the intensity of NIR-II luminescence, resulting a higher resolution in in vivo tumor imaging (Cao et al., 2020).

There are some interesting new studies for Ln-UCNPs outside in vivo imaging. Giri et al. coated Ln-UCNPs with oleylamine to obtain OA-Ln-UCNPs, and then further processed it to make a Ln-UCNPs oleogel with better skin permeability. The loading of Ln-UCNPs in the oleogels was varied to study the relationship between concentration and fluorescence intensity. For in vitro experiments, the Ln-UCNPs oleogel could penetrate the skin more deeply than free OA-Ln-UCNPs and be used as a skin tissue imaging agent under near-infrared excitation. Xu and co-workers reported the application of Ln-UCNPs in plant cell imaging, whereby LiErF4:1%Tm³⁺@LiYF4 with a core-shell structure could enter the cell membrane easily and emit bright red light (Qiao et al., 2021).

Computed tomography (CT) is based on the difference in the absorption and transmittance of X-rays among various tissues of the human body. The data is scanned by an instrument and processed to determine the pathological condition (Pfeiffer, 2018). Lanthanides have high X-ray attenuation coefficients (Issa et al., 2018), for example, the atomic number and electron density of Lu and Yb are greater than iodine which is currently used in CT. Du et al. reported the synthesis of core-shell nanoparticles NaYF₄:Yb/Er@NaLuF₄:Nd/Yb@NaLuF₄ and surface modification of chitosan. Next, Ag₂Se was grown in situ to form NaYF₄:Yb/Er@NaLuF₄:Nd/Yb@NaLuF₄@CS@Ag₂Se. In vivo imaging experiments with these agents demonstrated potential for clinical CT (Du et al., 2020). Bismuth doping of materials significantly improves CT imaging as Bi has better X-ray attenuation ability compared to lanthanides. You et al. reported the synthesis of a porous BiF3:Yb, Er nanomaterial that generated an in vivo CT signal as demonstrated with concentration dependence. The CT value curve showed that the Hounsfield unit (HU) value of the sample was higher than observed in commercial Iohexol (Zhao et al., 2020). Gao and co-workers reported the synthesis of BaYF5 with different bismuth doping ratios: Yb, Er, Bi-x (x = 0–3). Under the excitation of a 980 nm laser, the up-conversion luminescence was enhanced with increasing Bi content, reaching a maximum at x = 2.5. Then Ln-UCNPs was coated with citrate for biological imaging. Both in vitro and in vivo experiments demonstrated that the Ln-UCNPs can be successfully used in X-ray CT imaging by accumulating at the tumor site (Luo et al., 2020).

Magnetic resonance imaging is a technique in which radio frequency pulses are applied to generate structural information (Tirotta et al., 2015; Clough et al., 2019). The signal is generated from relaxation of nuclei from the excited state to equilibrium over the relaxation time. There are two relaxation times, labeled T1 and T2, where T1 is the spin-lattice or longitudinal relaxation time and T2 is the spin-spin or transverse relaxation time. Therefore, MRI is divided into T1 MRI and T2 MRI. The lanthanide gadolinium is the main contrast agent for T1 MRI due to its paramagnetic properties (Li et al., 2014; Yang et al., 2016; Tse et al., 2019). Liu et al. reported a T1-weighted nanocontrast agent with smart MRI switch based on NaGdF₄. Ultra-small NaGdF₄ and pH-sensitive CaCO₃ generated self-assembled bare self-assembled nanoparticles (BSNPs) in organic solvents (Figure 8). The addition of a tumor targeting coating on the surface effectively guided the BNSPs to the tumor location, and then CaCO₃ reacted with the acidic environment to release NaGdF₄ to achieve MRI with 60 times higher contrast compared to the commercial contrast agent Magnevist (Yi et al., 2019). Superparamagnetic Fe₃O₄ nanoparticles combined with Ln-UCNPs are often used in T2 MRI. Li et al. synthesized Fe₃O₄@NaGdF₄:Yb:Er-HMME with a core-shell structure, which was used for both treatment and imaging. The super paramagnetism of the sample was first confirmed, and its T2-weighted MRI performance was studied. Compared with the commercial T2 contrast agent Feridex, the samples performed better, and were effective for use in in vivo T2 MRI (Wang et al., 2019b).

Single-Photon Emission Computed Tomography (SPECT) and Positron Emission Tomography (PET) are two techniques in nuclear medicine. PET is the only imaging technique that can interrogate biomolecular metabolism, receptors, and neuromediator activity in vivo. Generally, substances necessary for metabolism, such as glucose, are labeled with short-lived radionuclides such as ¹⁸F and ¹¹C. After injection into the human body, metabolic activities are reflected by the accumulation of the radiolabeled probes to enable diagnosis. Fang et al. (2020) used cancer cell membrane-modified NaGdF₄:Yb,Tm@NaGdF₄ for UCL/MRI/PET trimodal tumor imaging and successfully differentiated triple-negative breast cancer subtypes MDA-MB-231 and MCF-7. Sun et al. (2011) used an efficient strategy for labeling Ln-UCNPs with ¹⁸F, and successfully applied the materials in sentinel lymph nodes mapping with PET imaging and detection. The materials were realized by the reaction between rare Earth cations and fluoride ions. The process was simple, fast, and efficient as no organic reagents were applied.

The principle of SPECT is to label probes with short half-life nuclides and inject them intravenously. The nuclides emit γ-rays through decay, and the γ-rays are then converted into electrical signals and input into a computer for tomography reconstruction. A cross-section or three-dimensional image reflecting the physiological condition of organs in the human body can be obtained. Li et al. (2020b) prepared radioactive PEG-modified NaYF₄:Yb, Er, Sm. These 10-nm nanoparticles were detected in kidney and urine by SPECT imaging and gamma counter analysis, confirming the potential for these probes as a biodistribution markers (Cao et al., 2013). Ma et al. (2021b) prepared a platelet membrane-coated nanostructure (PM-PAAO-Ln-UCNPs) containing Ln-UCNPs and Ce6 photosensitizer (PAAO = poly(noctylamine) acrylate), and injected them into mice models. SPECT/CT dual-mode imaging was performed and the precise location of an atherosclerotic plaque was demonstrated.

The pH of the cell can reflect its condition; for example, abnormal cells are acidic. Furthermore, as some viruses and germs are most active under acidic conditions, (White et al., 2017) it is important to monitor intracellular pH. Ratiometric (dual color) Ln-UCNPs-based pH ratiometric sensors can be prepared by first analyzing the emission spectrum of Ln-UCNPs to ensure that it has a pH-insensitive component to serve as a reference, and then coupling it to a fluorescent pH indicator. Proper spectral matching results in fluorescence resonance energy transfer that can generate pH-dependent emission. The Schaferling group coupled Ln-UCNPs to a fluorescent pH-dependent dye pHrodoTM Red. The NaYF₄:Yb³⁺, Er³⁺ material emits at 550 and 660 nm under laser excitation at 980 nm. As the emission peak at 550 nm was found to be invariant to changes in pH, it was used as a reference signal. The dye pHrodoTM Red emitted at 590 nm with an intensity that is dependent on pH. As a result, the combination of the two chromophores created a ratiometric fluorescence probe that displayed a linear response to pH over the range 3–6.7 (Arppe et al., 2014). Likewise Resch-Genger et al. combined NaYF4:Yb³⁺, Tm³⁺ with a pH-sensitive BODIPY dye to create a ratiometric pH sensor (Figure 9). Excitation at 980 nm resulted in 475 nm emission of Tm³⁺ that was absorbed by the dye, while the pH-insensitive 648 nm emission of Tm³⁺ was used as a calibrant against the 528 nm emission of BODIPY. This two-component sensor was successfully applied for pH monitoring in Escherichia coli (Radunz et al., 2019). Ln-UCNPs can also be coupled to pH-dependent fluorescent proteins to create ratiometric sensors. Recently, it was reported that Ln-UCNPs were combined with mOrange fluorescent protein. Excitation at 980 nm resulted in UCL green emission by the Ln-UCNPs, which subsequently excited the mOrange fluorescent protein. The ratio of the pH independent Ln-UCNPs emission at 655 nm to the pH- dependent emission of mOrange fluorescent protein was a quantifiable metric that was shown to have good stability and reversibility (Ghosh et al., 2020).

Sensitive, convenient, and biocompatible temperature sensors are needed for biological studies (Tran Quang et al., 2016; Ge et al., 2020). Some rare Earth particles have temperature sensitive luminescence properties, which makes them good candidates for biological thermal sensing (Du et al., 2014; Zheng et al., 2014; Wang et al., 2015; Du and Yu, 2017). Lin et al. synthesized doubly-doped NaLuF4:Mn²⁺, Ln³⁺(Ln³⁺ = Yb³⁺, Er³⁺, Tm³⁺), which have red/NIR dual emission that can be enhanced by the SPR effect of proximal Au nanoparticles. Embedding both these materials into the thermoresponsive polymer poly(N-isopropylacrylamide) (PNIPAM) resulted in a temperature dependent modulation of the Ln-UCNPs and Au nanoparticle distance. The effect was to modulate the red to NIR emission ratio, which was the metric of the temperature-sensitive sensor that had a resolution of 0.9°C (Xiao et al., 2014). Shahzad et al. (2019) co-doped microfibers with LiYF₄:Yb³⁺/Er³⁺, polymethyl methacrylate, and silver to create temperature sensors. The temperature dependent ratio of the emission intensity at 522 nm and 541 nm of the Ln-UCNPs was quantified over the range of 303–348 K. Doping with Ag was shown to significantly improve the photostability and temperature response of the composite (Shahzad et al., 2019). A study on the temperature sensitivity of ZnO:Yb³⁺/Tm³⁺ has been reported. The Ln-UCNPs was excited using a 980 nm laser to produce blue and red UCL emission. The UCL decreased at lower temperatures in the range of 300°C–780°C. The ratio of the intensities of the blue and red emission was modulated by 2.1% K⁻¹ at 293 K (Li et al., 2017a). Zhong et al. synthesized a new type of 8.5 nm × 12.5 nm nanoparticle of NaY(WO4)2:Er³⁺, Yb³⁺ that were shown to be temperature sensitive over the range 293 K–503 K (Lin et al., 2019). In addition to explore the relationship between luminescence of Ln-UCNPs and temperature, researchers have combined various fiber optic probes and temperature-sensitive Ln-UCNPs. Kumar et al. designed Ln-UCNPs coated with polydimethylsiloxane (PDMS) to obtain better fluorescence emission. The pure Ln-UCNPs and Ln-UCNPs-PDMS composite materials were coated on optical fibers for temperature sensing. The sensor coated with composite material displayed a linear response from 295 to 473 K (Kumar et al., 2020). A recent report demonstrated the coating of a temperature-dependent Ln-UCNPs onto the surface of spider silk, a natural optical fiber, to construct a temperature sensor with good biocompatibility. The change in fluorescence intensity of Ln-UCNPs reflected the temperature change of cancer cells. In addition, the sensor successfully detected temperature changes during apoptosis (Gong et al., 2021). Meiling et al. designed a lanthanide nanoscale temperature measurement system that can be used for the diagnosis of in vivo inflammation. The structure included an inert core, an active shell and an inert shell. The thermosensitive lanthanide elements were localized in the intermediate shell to shield from interference of the bioactive environment. This ternary structure enabled nanothermometers to continuously measure temperature changes of up to 4 mm depth in biological tissues, with high temperature sensitivity over a physiological temperature range of 10°C–64°C (Tan et al., 2020b). Although Ln-UCNPs are not the only material used for temperature sensors, their use imparts unique advantages. Ln-UCNPs have adjustable excitation wavelengths and can be excited by near-infrared light, making such temperature sensors beneficial for in vivo applications. Additionally, Ln-UCNPs have multi-color luminescence, which enables a wide selection of emission for construction of a temperature sensor.

Gas molecules are of great significance in many biological processes. For example, O₂ is important for maintaining metabolism (Mates et al., 2012). CO₂ can regulate breathing and the acid-base balance in the body. NO regulates cardiovascular function and improves the immunity of white blood cells (Carpenter and Schoenfisch, 2012; Lundberg et al., 2015; Farah et al., 2018). As a result, the sensing of gas molecules can elucidate the internal physiological behaviors of organisms. In 2010, Achatz et al. (2011) reported a CO₂ gas sensor based on Ln-UCNPs for the first time. In their system bromothymol blue was used as the luminescence intensity modifier of Ln-UCNPs on polystyrene. Specifically, bromothymol blue the absorption of bromothymol blue quenched the emission of the Ln-UCNPs; however, the presence of acidic CO₂ changed the pH which instigated a color change. Thus, when the CO₂ concentration increased, the absorption of bromothymol blue was minimized which resulted in higher intensity Ln-UCNPs fluorescence that enabled a quantitative detection of CO₂ with a detection limit of 0.11% (Ali et al., 2010). The same group created other gas sensors using Ln-UCNPs. They reported the first application of NaYF₄:Yb, Tm excited by near-infrared light as an O₂ sensor. First, an iridium (III) oxygen probe, Ln-UCNPs, and ethyl cellulose were dissolved in tetrahydrofuran. The solvent was evaporated to yield a sensor film. The Ln-UCNPs was excited by a 980 nm laser and emitted at 455 nm and 475 nm. These two emission peaks overlapped the absorption of the iridium complex at 468 nm. Therefore, Ln-UCNPs acted as a nanolamp in the sensor. The fact that the iridium complex’s emission at 568 nm is quenched by O₂ enabled quantitatively oxygen detection (Achatz et al., 2011).

Although the content of metal ions in organisms is small, they play an important role in maintaining the acid-base balance of cells and organisms and other metabolic activities, and are components of many complex biological compounds. The luminescence properties of Ln-UCNPs show great advantages for metal ion detection. Many studies have demonstrated that ion sensors based on Ln-UCNPs have high sensitivity and selectivity, the results from which can be visualized for convenient operation. Iron directly participates in the transport and storage of oxygen. It is a component of hemoglobin, myoglobin and cytochrome, and is necessary for many metabolic processes (Abbaspour et al., 2014; Sangkhae and Nemeth, 2017). The Lee group reported that adrenaline-modified NaYF₄:Yb, Tm was used for intracellular Fe³⁺ detection. PEP can complex with Fe³⁺, and the energy transfer with the Ln-UCNPs occurred through non-radiative electron transfer and energy return (EBT), resulting in reduced Ln-UCNPs emission at 474 nm. The detection limit of the Fe³⁺ sensor was 0.2 μM over a range of 1–10 μM (Gerelkhuu et al., 2021). The content of zinc in the human body can affect the activity of many enzymes, and as a result Zn²⁺ has an important role in human health (Maret, 2013). Chang et al. synthesized a Zn²⁺ sensor composed of a Ln-UCNPs and a Zn²⁺ sensitive dye.

NaYF₄:Yb/Tm@NaYF₄ has a multi-peak emission; the blue component at 475 nm was within in the absorption range of the dye while the 654 nm emission was not affected. When Zn²⁺ was added, the absorption of the dye shifted to 360 nm, which led to an increase in the ratio of I475 nm/I654 nm. The sensor successfully detected Zn²⁺ in a live animal model of zebrafish (Peng et al., 2015).

Copper is an indispensable component in blood and participates in hematopoietic process and iron metabolism. It was reported that core-shell Ln-UCNPs were electrostatically adsorbed onto flexible carbon fiber cloth (CFC) to create Cu²⁺ sensors (Figure 10). The absorption of Cu⁺ and Cu²⁺ coincided with the emission of Ln-UCNPs, which is a sensing mechanism. It was the first time that electrochemical technology was used to improve the sensing performance. Cu²⁺ accumulated when a voltage of 0.3 eV was applied. CFC reduced the quenching of Ln-UCNPs in water. The synergy of the electrochemical technology and the CFC protective layer resulted in a detection limit of 82 ppb (Wong et al., 2019). Trace fluoride can promote the normal development of teeth and bones, but excessive fluoride causes dental and skeletal fluorosis. Dual-functional gallic acid-Fe(III) modified Ln-UCNPs was reported with a 654 nm emission that was quenched by the Fe-complex. The presence of F⁻ destroyed the Fe-complex, which imparted a sensing mechanism between the UCL and F⁻ ion analyte (Ma et al., 2017).

Recently there have been many reports on the use of Ln-UCNPs for the detection of miRNA and other biologically active molecules (Yuan et al., 2015; Li et al., 2016). Trypsin is an activating enzyme that plays an important role in food digestion and has anti-inflammatory and swelling functions (Plattner and Noe, 2015; Wattanasiritham et al., 2016). Guo et al. synthesized Ln-UCNPs-peptide-AuNP for the detection of trypsin and its inhibitors. The peptide, DDDDARC, is sensitive to trypsin. In the initial state, the emission of UCL was quenched by the Au NP due to Förster Resonance Energy Transfer (FRET) energy transfer. After adding trypsin the peptide was cleaved and UCL was restored. The detection limit of the trypsin sensor was 4.15 ng/mL (Wu et al., 2017). Cytochromes are involved in cell redox reactions and take part in cell energy transfer (Zanger and Schwab, 2013). Wang et al. attached a Cy3-labeled aptamer to the surface of a Ln-UCNPs wrapped with PDA (Figure 11). The aptamer responded to cytochrome c to trigger changes in the fluorescence intensity of Cy3, and the internal UCL served as a reference signal. The sensor reflected the level of Cytc through a ratiometric fluorescence signal, with a detection limit of 20 nM over a range of 50 nM to 10 μM (Ma et al., 2017).

Recent studies have demonstrated that a single sensor can be used for the simultaneous detection multiple biomolecules. Xu et al. developed an Au-Au-Ln-UCNPs with an aptamer with sensitivity for both alpha-fetoprotein (AFP) and mucin 1. The sensor generated both Raman and fluorescence signals. Mucin 1 concentration was detected through the change of surface enhanced Raman scattering intensity, and AFP was sensed by the change of fluorescence intensity. The detection limits of both proteins were at an attomolar level (Qu et al., 2017).

Thrombin acts on the last step of the blood coagulation process. It can be used to stop bleeding and is a relevant marker for tumor diagnosis. Prostate-specific antigens are abundantly present in prostate tissue and semen, with extremely high tissue organ specificity, and are currently the first-choice marker for the diagnosis of prostate cancer. Kuang et al. used a Raman signal and fluorescence of Au-Ln-UCNPs in conjunction with aptamers to respond to thrombin and prostate specific antigen (PSA). The signal intensity of SERS was affected by the concentration of thrombin. The fluorescence signal was affected by PSA, and the detection limit was 3.2 × 10⁻²⁰ M (Hao et al., 2017).