Abstract
Photodynamic therapy (PDT) is a promising anticancer treatment because it is patient-friendly and non-invasive. Methyl pyropheophorbide-a (MPPa), one of the chlorin class photosensitizers, is a drug with poor aqueous solubility. The purpose of this study was to synthesize MPPa and develop MPPa-loaded solid lipid nanoparticles (SLNs) with improved solubility and PDT efficacy. The synthesized MPPa was confirmed 1H nuclear magnetic resonance (1H-NMR) spectroscopy and UV–Vis spectroscopy. MPPa was encapsulated in SLN via a hot homogenization with sonication. Particle characterization was performed using particle size and zeta potential measurements. The pharmacological effect of MPPa was evaluated using the 1,3-diphenylisobenzofuran (DPBF) assay and anti-cancer effect against HeLa and A549 cell lines. The particle size and zeta potential ranged from 231.37 to 424.07 nm and − 17.37 to − 24.20 mV, respectively. MPPa showed sustained release from MPPa-loaded SLNs. All formulations improved the photostability of MPPa. The DPBF assay showed that SLNs enhanced the 1O2 generation from MPPa. In the photocytotoxicity analysis, MPPa-loaded SLNs demonstrated cytotoxicity upon photoirradiation but not in the dark. The PDT efficacy of MPPa improved following its entrapment in SLNs. This observation suggests that MPPa-loaded SLNs are suitable for the enhanced permeability and retention effect. Together, these results demonstrate that the developed MPPa-loaded SLNs are promising candidates for cancer treatment using PDT.
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Introduction
Photodynamic therapy (PDT) is one of the anticancer treatment strategies that is patient-friendly, noninvasive, and highly localized1. A photosensitizer (PS) essentially is a PDT drug that exerts pharmacological effects in the presence of light of an appropriate wavelength. Upon irradiation with light, the PS generates reactive oxygen species, particularly singlet oxygen (1O2), that triggers cancer cell death1,2,3. PS are preferentially localized in tumor sites that are harmless to adjacent healthy cells4,5. PDT offers the advantages of extremely low systemic toxicity and excellent function-sparing treatment as compared to conventional cancer treatment strategies, including chemotherapy, surgery, radiotherapy, and immunotherapy1,2,6,7,8.
Researchers continue to search for an ideal PS that interacts with light of a relatively long wavelength. Light with long wavelengths effectively penetrates the human body and can treat deeply placed tumors2,9,10. Methyl pyropheophorbide-a (MPPa), one of the chlorin class of PSs, is a second-generation PS with relatively long wavelength absorption as compared with the porphyrin class of the first-generation PS11. The molecular weight of MPPa is 548.7 g/mol.
MPPa has relatively high hydrophobicity, leading to low bioavailability, as it suffers significantly from administration challenges2,7,9,12. Various approaches have been proposed to enhance the solubilization of poorly water-soluble drugs, including conjugation of PS to water-soluble polymers13, entrapment of PS into polymer-based particles9,14, amorphization9,15 and nanonization2,9,16. However, considering the time-consuming amorphization process and the concerns of storage stability attributed to the hygroscopic properties of polymers, it is important to investigate pharmaceutical technologies that could enhance the solubility of MPPa9,17.
Solid lipid nanoparticle (SLN) is a promising drug delivery system for enhancing aqueous solubility and stability of poorly water-soluble drugs2,7,9,18,19. In the SLN system, a hydrophobic drug is molecularly dispersed in a solid lipid matrix as an oil (O) phase, and the drug-dissolved O phase is then stably dispersed in water by forming an oil-in-water (O/W) phase9,18,20. The solid lipid of the SLN system physically protects the entrapped drug from external environments (light, pH, and atmospheric moisture)21,22,23,24. In cancer therapy, conventional pharmaceutical strategies have used the enhanced permeability and retention (EPR) effect for passive targeting of agents25,26. Anticancer drugs up to a size of 400 nm can spontaneously accumulate in tumors with leaky vasculature27,28,29.
We hypothesized that SLN can improve the solubility and pharmacological effects of MPPa based on the EPR effect used itn cancer therapy. We synthesized MPPa from chlorophyll and fabricated the MPPa-loaded SLN. The structure of the synthesized MPPa was confirmed using 1H nuclear magnetic resonance (1H-NMR) spectroscopy, and the pharmaceutical characteristics of MPPa-loaded SLNs were determined using particle characteristics and Fourier transform infrared spectroscopy (FTIR). We assessed the PDT efficacy by analyzing 1O2 production using 1,3-diphenylisobenzofuran (DPBF) as a non-biological assay and by evaluating the viability of two cancer cell lines (HeLa from human cervical carcinoma and A549 from human lung carcinoma) using the WST biological assay.
Materials and methods
Materials
Phosphate-buffered saline (PBS), methylene blue (MB), and chloroform were purchased from Sigma-Aldrich (St. Louis, MO, USA). Palmitic acid (PA) and stearic acid (SA) were supplied by SAMCHUN (Pyeongtaek, Korea). Glycerol monostearate (GMS) was obtained from Kanto Chemical Co, Japan. Inc. (Tokyo, Japan), and Poloxamers (PX) 188 and PX 407 were procured from BASF (Ludwigshafen, Germany). Tween 80 (TW 80) was purchased from Dae Jung Co., Ltd. (Busan, Korea) and chlorophyll-a paste from Shandong Lanmo Biotech Co. Ltd. (Shanghai, China). Methylene chloride (CH2Cl2, MC) and DPBF were supplied by Duksan Co. Ltd. (Gyeonggi-do, Korea) and TCI Chemicals (Tokyo, Japan), respectively. Dulbecco’s modified Eagle’s medium (DMEM) was provided by WelGENE (Gyeongsan, South Korea), and penicillin–streptomycin solution (100 ×) and fetal bovine serum (FBS) were purchased from BioWest (Nuaillé, France). The cancer cell lines (HeLa and A549) were obtained from the Korea Cell Line Bank (Seoul, Korea), and the Quanti-MAX WST-8 assay kit from Biomax (Seoul, Republic of Korea). High-performance liquid chromatography (HPLC)-grade methanol (MeOH) was purchased from Honeywell (Seelze, Germany). All other chemicals used were of HPLC grade.
Synthesis of MPPa
Methyl pheophorbide-a (MPa) was extracted from chlorophyll-a paste according to a previously reported procedure (Fig. 1A)30. The synthesized MPa (1 g) was dissolved in 2,4,6-collidine (2,4,6-trimethylpyridine, 100 mL) and refluxed for 3 h, followed by cooling, evaporation of collidine, and washing with 2% HCl/MC (1:1). The obtained organic layer was evaporated and the residue was separated by column chromatography using 2% acetone/MC as the eluent to obtain pure MPPa.
Preparation of MPPa-loaded SLNs
MPPa was loaded into SLN using a modified oil-in-water (O/W) emulsion method31. To prepare the O-phase, MPPa was added to the heated lipid at 10 °C above the lipid melting point. Subsequently, the O phase was added to the surfactant-dissolved W phase and homogenized using a polytron homogenizer (PT 3100) (Kinematica Instruments, Luzerne, Switzerland) at 1000 rpm to obtain an O/W emulsion. The obtained O/W emulsion was subjected to sonication to prepare SLN using a probe sonicator (Scientz-IID, Ningbo, China) at 300 W for 15 min with a 5 s pulse-on and a 5 s pulse-off period. The different compositions of MPPa-loaded SLN are shown in Table 1.
NMR spectroscopy of MPPa
All 1H-NMR experiments were performed using a Varian spectrometer (500 MHz, CDCl3) at the Biohealth Products Research Center, Inje University31,32.
Development of analytical method for MPPa
The MPPa concentration was determined using a UV–Vis spectrophotometer (S-3100, Scinco, Seoul, Korea) at ambient temperature31,32. To determine the maximum absorption wavelength of MPPa, the absorption spectrum was measured in the wavelength range 300–800 nm. The solvent that demonstrated the best characteristics for this method was MeOH. A standard stock solution was prepared by dissolving 2 mg of an accurate amount of MPPa in 20 mL of MeOH.
The standard stock solution was diluted with MeOH to obtain final concentrations of 1–20 ppm, and five-point linearity was determined. Standard solutions of different concentrations were prepared. Calibration curves and concentration versus absorbance units were constructed for each drug.
The precision of the test method was determined by performing an assay with six replicates of samples at test concentrations, and the relative standard deviation (RSD) of the assay results was calculated.
To study the accuracy of the method, recovery studies were performed by adding a known quantity of the standard to the pre-analyzed sample. The recovery was performed at 0%, 25%, and 100% levels, and the contents were measured from the respective UV–Vis absorption spectra.
Determination of nanoparticle size, polydispersity index (PDI), and zeta potential for MPPa-loaded SLNs
The particle size and PDI of the prepared SLNs were determined at 25 °C by dynamic light scattering using a Zetasizer Nano ZS (Malvern Instruments Ltd., Worcestershire, Malvern, UK)31,32,33. The zeta potential of SLNs was estimated from the electrophoretic mobility of the particle surface using a Zetasizer Nano ZS. The samples were diluted 10 times with distilled water (DW) before the measurement. The instrument was equilibrated before each measurement. Each value reported is the average of three measurements.
Determination of drug-loading capacity MPPa-loaded SLNs
The entrapment efficiency (EE) and loading amount (LA) of MPPa-loaded SLNs were determined by centrifugation29. SLN preparations were diluted 10 times to a final volume of 1 mL and then gently vortexed. The suspension was then centrifuged at 190 g at 4 °C for 1 h. The free drug concentration in the supernatant was analyzed using a UV–Vis spectrophotometer. EE and LA were calculated using Eqs. (1) and (2), respectively.
In vitro MPPa release studies
An in vitro MPPa release study was performed using the dialysis-bag method. Dialysis bags (Spectrum Laboratories, Inc., Compton, CA, USA) with a molecular weight of 10 kDa were soaked in DW for 12 h before the experiment34. A predetermined amount of each test substance was soaked in dialysis bags and both ends were sealed using a string. Dialysis bags were immersed in 70 mL vials containing 50 mL of receptor medium (PBS, pH 7.4). The vials were then placed in a shaking incubator (JSSI-100 T, JS Research Inc., Gongju, Korea) and shaken at 100 rpm and 37 ± 0.5 °C. At predetermined time intervals (1, 2, 4, 8, 12, 24 and 48 h), aliquots of 1 mL were withdrawn from the vial, passed through 0.45 μm membrane filters (SFCA Syringe Filters, Corning Inc., NY, USA), and immediately analyzed using a UV–Vis spectrophotometer.
The drug release kinetics models
To explain the mechanism of MPPa releases from the SLNs, the MPPa release profiles of the SLNs were analyzed with various models of release kinetics including zero-order, first-order, Higuchi, and Korsmeyer-Peppas models using Eqs. (3), (4), (5) and (6), respectively.
where Qt is the amount of drug release at time t, Q0 is the initial amount of drug in formulations, K0, Kt, KH are release rate constants, C0 is the initial concentration of drug.
Photostability studies
The photostability of MPPa in SLNs was determined by comparison with MPPa in 0.1% MeOH solution29. The photostability of MPPa was monitored by recording its absorption spectrum at 700 nm. Briefly, 20 mL of MPPa or MPPa-loaded SLNs in a 0.1% MeOH solution (4.0 ppm) was irradiated with a light-emitting diode (LED) at different time intervals (0, 10, 20, 30 and 40 min). MPPa was then extracted from the formulations by adding 1 mL hexane to melt the lipids, followed by vortexing. A 0.1% MeOH layer containing the extracted MPPa was filtered through 0.22 μm filters, and the UV–Vis spectrophotometer was measured.
1O2 Photogeneration
1O2 photogeneration study was determined using DPBF. DPBF, a selective 1O2 acceptor, is bleached upon reaction with 1O2, leading to a decrease in the intensity of the DPBF absorption band31,32. Each sample (1 μM) with 50 μM of DPBF in DMSO was used to evaluate photogeneration. The negative control (NC) and positive control (PC) contained 50 μM DPBF and 1 μM MB with 50 μM DPBF, respectively. All samples prepared in the dark were placed in a 48-well plate and covered with an aluminum foil. The plate was irradiated (2 J/cm2) with an LED (645‒710 nm) for 15 min. The absorbance of each sample was measured at 418 nm using a microplate reader (Synergy HTX; BioTek, Winooski, VT, USA).
The 1O2 quantum yields of MPPa and all formulations were determined using DPBF as a probe and MB as the standard with that calculation of Eq. (7)35,36.
ɸΔ: singlet oxygen quantum yield, ɸSΔ: singlet oxygen quantum yield of MB equal to 0.596, ɣSΔ: photodynamic activity of MB, and ɣΔ: photodynamic activity of specimen.
In vitro photoirritation study using human tumor cells
The anticancer efficacy of PDT with MPPa was evaluated by investigating the cytotoxic effects of each component of SLNs in tumor cell lines after photoirradiation29,34. Two cell lines (HeLa from human cervical carcinoma and A549 from human lung carcinoma) were seeded into 48-well plates at 2 × 104 cells/well, and the number of cells was calculated using a hemocytometer. Prior to each experiment, the cells were incubated for 24 h at 37 ± 0.5 °C in a humidified atmosphere with 5% CO2. Various concentrations (1, 2.5, 5, and 10 μM) of each sample were then added to each well. After 24 h, the exposed cells were rinsed with sterile PBS and incubated with 200 µL/well of the growth medium. The cells were then irradiated (2 J/cm2) with LED at a distance of 20 cm for 15 min. The treated cells were incubated for 24 h at 37 ± 0.5 °C and 5% CO2 for the WST reduction experiment.
Viability of cancer cells
Cytotoxicity was determined by measuring the dehydrogenase activity of viable keratinocytes at 24 h after incubation. Activity was determined after the incorporation of WST, as previously described37. Each cell line was treated with 100 µL/well of a 10% WST solution for 1 h. The WST concentration was measured by determining the optical density (OD) at 450 nm using a microplate reader.
Each experiment was conducted in at least three wells of a plate. After subtracting the blank OD from all raw data, the mean OD values ± standard deviations (SDs) were calculated using three measurements per test substance, and the percentage of cell viability relative to that of the NC was expressed using Eq. (8). The NC value was set at 100%.
Statistical analysis
Three independent experiments were performed for all analyses. The presented data (mean ± SD) were compared using a one-way analysis of variance and Student’s t-test. Statistical significance was set at p < 0.05.
Results and discussion
NMR spectroscopy of MPPa
The structure of MPPa was characterized by 1H-NMR spectroscopy. Figure 1B shows the 1H-NMR spectrum of MPPa. 1H-NMR (500 MHz, CDCl3, 25 °C, TMS): δ 9.48 (d, J = 12.0 Hz, 1H, 10H), 9.37 (d, J = 10.2 Hz, 1H, 5H), 8.54 (s, 1H, 20H), 8.03–7.95 (m, 1H, 31H), 6.30 (d, J = 17.9 Hz, 1H, 32H), 6.17 (d, J = 11.6 Hz, 1H, 32H), 5.28 (d, J = 19.5 Hz, 1H, 132H), 5.13 (d, J = 19.5 Hz, 1H, 132H), 4.48 (m, 1H, 18H), 4.30 (m, 1H, 17H), 3.69 (m, 2H, 81CH2), 3.66, 3.40, 3.23 (each s, 9H, CH3), 2.69 (m, 1H, 172CH2), 2.29 (m, 2H 171CH2), 2.04 (m, 1H, 172CH2), 1.82 (d, J = 7.4 Hz, 3H, 181CH3), 1.69 (t, J = 7.6 Hz, 3H, 82CH3), − 1.70 (br, 2H, NH). Our results revealed that the peak for -OCH3 (134H at 3.88 ppm as previously reported by us) in MPa disappeared after elimination of –COOCH3, and one proton signal of 132 at 5.13 ppm appeared that confirmed the formation of reduced five-membered ring in MPPa32.
Development of analytical method for MPPa
We obtained absorption spectra using a UV–Vis spectrophotometer to determine the specific absorption wavelength of MPPa (Fig. 2A). The specificity of MPPa was determined using MPPa standard stock solution, MPPa-loaded SLN, and placebo SLN (SLN without MPPa). The UV–Vis spectra of MPPa demonstrated that the maximum absorption wavelength was 667 nm. The placebo SLN had no interference spectra with that of MPPa. Therefore, we analyzed MPPa at 667 nm.
To calculate MPPa, we prepared a calibration curve using five standard stock solutions in a concentration range of 1–20 ppm. Figure 2B shows that the correlation coefficient obtained via the linear regression analysis was 1.
A precision study was performed to determine the closeness of the agreement for the same concentration with repeated measurements. The precision results are expressed as the RSD of repeatability. MPPa results demonstrated that the RSD (%) value of recovery was 1.06% (Table 2), which indicated the high precision of the proposed analytical method.
We determined the accuracy via the developed analysis of MPPa to determine the closeness of agreement between the test results and a conventional true or accepted reference value. The recovery of MPPa was calculated and expressed as RSD. The RSD (%) values resulting from the accuracy were 1.26%, 0.42%, and 0.36%, respectively, as shown in Table 3.
Particle characterization of MPPa-loaded SLNs for MPPa-loaded SLNs
Considering particle characterization, nanoparticle size, PDI, and zeta potential were determined to investigate the effects of different lipids and surfactants. Particle size is an important parameter in cancer therapy and is based on the EPR effect as a passive targeting strategy26,38. For nanoparticles, the zeta potential is important because it indicates the electric surface potential on the particles that ensures particle stability18,39. The results of particle size, PDI, and zeta potential demonstrated that all the formulations ranged from 231.37 to 424.07 nm in size, had a PDI of 0.15 to 0.42, and zeta potential of − 17.37 to − 24.20 mV, respectively, as shown in Fig. 3A,B. The particle size and zeta potential of formulations prepared using PA, SA, and GMS (F1, F2, and F3) were 424.07, 406.63, and 284.90 nm and − 17.37, − 17.97 and − 23.33 mV, respectively. This observation suggests that lipids with long carbon chains have a high affinity for MPPa, resulting in a small particle size and high zeta potential. The high affinity of lipids for MPPa could facilitate interaction with each other rather than the outer water phase40,41,42. The results of particle characterization for F3, F4, and F5, which were fabricated using different surfactants, demonstrated that F3 had the smallest size and highest zeta potential. This result suggests that a hydrophilic surfactant stabilizes the interface between O and W in O/W emulsions39. The high hydrophilic-lipophilic balance (HLB) of a hydrophilic surfactant is more stable than that of a relatively low HLB value. The HLB values of PX 188, PX 407, and TW 80 were 29, 22 and 15, respectively. Therefore, we selected GMS as a solid lipid and PX 188 as a surfactant to prepare SLN.
Considering the effects of lipid and surfactant concentrations on F3 and F6 to F10, the results of particle characterization demonstrated that an increase in the concentration of GMS as a lipid led to an increase in the particle size. For the surfactant, an increase in the concentration of PX 188 led to a decrease in the particle size. This observation suggests that the concentration effect of lipids is associated with the increased volume of the lipid matrix23. An increase in the concentration of surfactant causes the interface between O and W in the O/W emulsion to be effectively stabilized (increased zeta potential), and consequently reduces the particle size and enhances the particle stability39.
Determination of the drug-loading capacity
Loading capacity (EE and LA) is a significant parameter in the formulation of lipid particle systems because it enhances the photostability of MPPa and avoids side-effects in the human body. Figure 3C,D show the EE and LA of MPPa-loaded SLNs. The EE and LA of all formulations were 73.49–78.73% and 1.54–7.11%, respectively. Among F1, F2, and F3, which were prepared using different lipids, F3 prepared from GMS showed the greatest loading capacity. This observation suggests that longer chain fatty acids have a high affinity for MPPa43,44,45, as mentioned in the particle characterization section. Regarding the effect of surfactants, F3 using PX 188 had a high amount of EE among F3, F4, and F5. This suggests that the high HLB value of the surfactant affected the stable dispersion of the MPPa-dissolved O phase into the W phase43,46,47. Regarding the effect of lipid and surfactant concentrations, an increase in the concentration of both increased EE owing to an increase in the volume of the lipid matrix and particle stability.
In vitro MPPa release studies
The release profile of MPPa-loaded SLNs was determined using the dialysis membrane method. The cumulative percentage release of MPPa-loaded SLNs was in the order F1 > F2 > F5 > F4 > F3 > F6 > F7 > F8 > F9 > F10. Among the formulations of F1 to F6, this order was the same as the particle size and reverse of the order of zeta potential (low stability), as shown in Fig. 3A and B. Thus, the large particle size and low stability of SLNs induced high drug release from SLNs after 48 h. The MPPa release from SLN exhibited a sustained release profile, as shown in Fig. 4. The sustained release of MPPa was biphasic, with a relatively burst and delayed release. The relatively burst release of F1–F6 and F7–F10 was observed over 12 and 8 h, respectively, followed by a sustained release for 48 h. This observation suggests that the relatively burst release is attributed to the adhesive MPPa on the particle surface (shell), whereas the sustained release is owing to the MPPa encapsulated into the particle core23. Concerning the short burst release of F7–F10, formulations with a high loading capacity are encapsulated in the particle core rather than the shell, which leads to a delayed release23. In this sense, the order of MPPa release was exactly the reverse of the order of EE, as shown in Fig. 3C.
The drug release kinetics models
The MPPa release results were analyzed using release kinetics models (zero order, first order, Higuchi, and Korsmeyer-Peppas). Table 4 demonstrates that Higuchi model is the highest correlation coefficients (R2) values. This suggests that MPPa was homogeneously loaded in entire lipid matrix of SLN. In this regard, MPPa release was dominated by diffusion and dissolution48,49.
Photostability studies
In PDT, the photostability of the PS is important because it is closely related to its pharmacological effect. Our results revealed that all formulations improved the photostability of MPPa (Fig. 5). The order of photostability after 40 min of irradiation was F10 > F9 > F8 > F7 > F6 > F3 > F4 > F5 > F2 > F1 > MPPa; this order was the exact reverse of that observed for the release profile of MPPa from SLNs shown in Fig. 4. The remaining concentration of MPPa from the MPPa solution was 57.97% and that from the formulations ranged from 74.67% to 91.43%. Thus, a solid lipid, as the main ingredient of SLN, physically prevents any interruption from environmental factors and maintains MPPa for a relatively long time22,23,50. The concentration effects of lipids and surfactants demonstrated that F7–F10 highly improved the photostability of MPPa probably because formulations with high loading capacity protect MPPa from environmental factors.
1O2 photogeneration
The efficacy of PDT was investigated using the DPBF assay where DPBF reacts with 1O2, which decreases the intensity of the DPBF absorption band51,52. We performed the DPBF assay with photoirradiation of the MPPa solution and all formulations to detect the generated 1O2, as shown in Fig. 6A. MB, a standard 1O2 sensitizer, was used as the PC. Additionally, high 1O2 quantum yields can promise high anti-cancer efficacy in PDT. The 1O2 quantum yields of MPPa and all formulations were measured and compared using DPBF as a probe and MB as the standard. The 1O2 quantum yield was calculated according to the literature35,36. DPBF results demonstrated that all formulations of SLNs exhibited better 1O2 photogeneration than the MPPa solution. This indicates that the PDT efficacy of all test substances was lower than that of MB. The MPPa-loaded SLNs improved the PDT efficacy of MPPa as compared to the MPPa solution. Thus, the aggregation of MPPa is prevented by applying SLN43,46. In addition, among the formulations of F1–F6, the order of the 1O2 photogeneration efficiency (1O2 quantum yields) was F1 (0.510) > F2 (0.505) > F5 (0.435) > F4 (0.410) > F3 (0.401) > F6 (0.365), which is the same as that observed for the release profiles in Fig. 4 and exactly opposite of the order reported for zeta potential and photostability in Figs. 3B and 5, respectively. Therefore, highly stable formulations afforded relatively low PDT efficacy among MPPa-loaded SLNs. The reason for this might be the environmental protective effect of the SLN system22,23.
In vitro photoirritation studies
Photocytotoxicity was evaluated as PDT efficiency using HeLa cells from human cervical carcinoma and A549 cells from human lung epithelial carcinoma. We selected F1, F3, F7, and F9 among the formulations based on particle size and EE results. We conducted cytotoxicity assay to determine the safety of the formulations because the PDT mechanism for 1O2 generation occurs under light2,3,44. Figure 6B and C shows the photocytotoxicity against HeLa and A549 cells. Under dark conditions, the viability of HeLa and A549 cells treated with 10 μM of the test substances ranged from 91.76 to 106.31% and 105.00 to 117.65%, respectively. These results revealed that MPPa and MPPa-loaded SLNs were not cytotoxic to HeLa and A549 cell lines.
Regarding the photocytotoxicity of MPPa, all test substances demonstrated anticancer effects depending on the cell type and concentration of MPPa. Four different concentrations of each test substance (1, 2.5, 5 and 10 μM) were used to estimate the 50% inhibitory concentration values (IC50). The results of IC50 are summarized in Table 5. The order of PDT efficacy was the same as the order of zeta potential and the opposite of the order of particle size as following: F3 (0.74 μM) > F7 (0.79 μM) > F9 (0.83 μM) > MPPa (0.97 μM) > F1 (1.38 μM) in HeLa cells; F3 (0.58 μM) > F7 (0.67 μM) > F9 (0.78 μM) > F1 (0.89 μM) > MPPa (0.96 μM) in A549 cells. Therefore, a small particle size with low aggregation (high zeta potential) results in better PDT efficiency. Regarding the effect of different lipids, F3 prepared using GMS showed high anticancer effects against both cell lines as compared with F1 prepared using PA. Moreover, although F7 and F9 had a higher MPPa loading capacity than F3, the PDT efficacy of F3 was higher than that of F7 and F9. Considering that the particle size of F3 was smaller than that of F7 and F9, the anticancer effects via PDT efficacy dominated the particle size rather than the drug-loading capacity3,53,54. In addition, the order of PDT efficacy was the same as that of release, except for F1. This is because the formulation with large particle size showed low zeta potential as a stability parameter that is affected by both high particle aggregation and fast drug release, as mentioned in the sections on particle size and drug release. Thus, F3 is a promising formulation for cancer treatment based on the EPR effect strategy among the tested substances.
Conclusion
In this study, we attempted to synthesize MPPa and fabricate MPPa-loaded SLNs as a promising cancer treatment for PDT to improve the photostability and pharmacological effects. 1H-NMR results showed that all proton signals were assigned, indicating the successful synthesis of MPPa. All MPPa-loaded SLNs displayed highly enhanced photostability and 1O2 photogeneration compared with free MPPa. In terms of PDT efficacy, our SLNs showed better anticancer effects than free MPPa against HeLa and A549 cells. In addition, the cytotoxicity study was performed under dark and light conditions, which ensured that the normal state of MPPa and MPPa-loaded SLNs was safe unless otherwise irradiated. Among F1, F3, F7 and F9 SLNs, use of lipid with longer carbon chain (GMS) generated smaller particle sizes of SLNs. In addition, a decrease of the lipid (GMS) concentration (among F3, F7 and F9) is important to decrease the particle size which induced an increase of the stability (increase of the zeta potential). Finally, F3 SLNs displayed the highest PDT efficiency against both cell lines, which might be attributed to the smallest particle size as well as the highest stability and loading amount even though the lower 1O2 photogeneration and entrapment efficiency. Therefore, we can make a conclusion that the anticancer efficacy of MPPa-loaded SLNs was dominated by particle size and stability rather than entrapment efficiency. Thus, these results showed that MPPa-loaded SLNs are promising anticancer agents for PDT.
Data availability
The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.
Abbreviations
- DPBF:
-
1,3-Diphenylisobenzofuran
- EE:
-
Entrapment efficiency
- EPR:
-
Enhanced permeability and retention
- FTIR:
-
Fourier transform infrared spectroscopy
- HLB:
-
Hydrophilic-lipophilic balance
- LA:
-
Loading amount
- LED:
-
Light-emitting diode
- MPPA:
-
Methyl pyropheophorbide-a
- NMR:
-
Nuclear magnetic resonance
- PDT:
-
Photodynamic therapy
- PS:
-
Photosensitizer
- RSD:
-
Relative standard deviation
- SLN:
-
Solid lipid nanoparticle
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Acknowledgements
Special thanks to Prof. Sung-Joo Hwang from Yonsei Institute of Pharmaceutical Sciences; College of Pharmacy, Yonsei University for measuring the drug release kinetics models and 1O2 quantum yields.
Funding
This research was supported by the BK21 FOUR (Fostering Outstanding Universities for Research, No.5199991614715), the National Research Foundation of Korea (NRF) grant, the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (MOE, Korea, NRF-2020R1I1A1A01060632), and the Korean government (MSIT) (NRF-2020R1F1A1070571). This work was supported by project for Collabo R&D between Industry, University, and Research Institute funded by Korea Ministry of SMEs and Startups in 2022 (S3248094). This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2018R1A6A1A03023718).
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Conceptualization: S.Y., I.Y., and W.K.L.; methodology: S.Y., T.H.L., and M.J.K.; resources: I.Y. and W.K.L.; writing-original draft preparation: S.Y.; funding acquisition: W.K.L.; supervision: W.K.L. All authors have read and agreed to the published version of the manuscript.
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Yeo, S., Lee, T.H., Kim, M.J. et al. Improved anticancer efficacy of methyl pyropheophorbide-a–incorporated solid lipid nanoparticles in photodynamic therapy. Sci Rep 13, 7391 (2023). https://doi.org/10.1038/s41598-023-34265-x
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DOI: https://doi.org/10.1038/s41598-023-34265-x
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