Sharma Surbhi, Dang Shweta
Department of Biotechnology, Jaypee Institute of Information Technology, Noida, India.
J Microencapsul. 2023 Nov;40(7):534-548. doi: 10.1080/02652048.2023.2244095. Epub 2023 Aug 23.
Present study focuses on the development of P80 coated PLGA Nanoparticles loaded with drugs, paroxetine (P80-Par-PLGA-NPs) and clonidine (P80-CLD-PLGA-NPs) for evaluation of Cellular Uptake & Cytotoxicity on Neuro-2a cells.
P80-Par-PLGA-NPs and P80-CLD-PLGA-NPs were developed and characterised for zeta size, potential, PDI, EE%, DL%, TEM, SEM, FTIR, DSC, i release, cytotoxicity, histopathological and cell uptake studies using rhodamine loaded P80-NPs.
Mean particle diameter of P80-Par-PLGA-NPs and P80-CLD-PLGA-NPs was 204; 182.7 nm, ZP of -21.8; -18.72 mV and 0.275; 0.341 PDI, respectively. TEM and SEM images revealed homogenous surface morphology. drug release showed sustained and complete release in 72 h. Cell viability (>90%) at C and no cytotoxicity in histopathology was observed. Significant higher uptake (96.9%) of P80-modified-NPS was observed as compared to unmodified-NPs (81%) (p < 0.05).
The finding clearly indicated a higher cell uptake of drugs via surface modified P80-coated PLGA-NPs as compared to unmodified particles.
本研究聚焦于负载药物帕罗西汀(P80 - Par - PLGA - NPs)和可乐定(P80 - CLD - PLGA - NPs)的P80包被聚乳酸 - 羟基乙酸共聚物纳米粒的研发,以评估其对神经母细胞瘤细胞(Neuro - 2a)的细胞摄取及细胞毒性。
制备P80 - Par - PLGA - NPs和P80 - CLD - PLGA - NPs,并对其进行表征,包括zeta粒径、电位、多分散指数(PDI)、包封率(EE%)、载药量(DL%)、透射电子显微镜(TEM)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、体外释放、细胞毒性、组织病理学以及使用罗丹明标记的P80 - NPs进行细胞摄取研究。
P80 - Par - PLGA - NPs和P80 - CLD - PLGA - NPs的平均粒径分别为204、182.7 nm,zeta电位分别为 - 21.8、 - 18.72 mV,PDI分别为0.275、0.341。TEM和SEM图像显示表面形态均匀。药物释放显示在72小时内持续且完全释放。在细胞毒性实验中观察到细胞活力在C时大于90%,组织病理学中无细胞毒性。与未修饰的纳米粒(81%)相比,观察到P80修饰的纳米粒摄取显著更高(96.9%)(p < 0.05)。
研究结果清楚表明,与未修饰的颗粒相比,经表面修饰的P80包被聚乳酸 - 羟基乙酸共聚物纳米粒对药物的细胞摄取更高。