Shweta Paroha, Ravindra Dhar Dubey, Juhi Verma, Vikas Jain, Saleem Akbar, Ashwini Kumar Mishra, S L Neha, Laxmi Rani, Aman Kumar Mahto, Parvat Kumar Sahoo, Rikeshwer Prasad Dewangan
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引用次数: 0
摘要
吉西他滨(Gem)是一种众所周知的抗肿瘤药物,用于治疗多种实体肿瘤。由于宝石的非选择性、半衰期短和耐药等特点,阻碍了宝石的临床应用,这就需要开发一种合适的新型制剂,可以选择性地靶向肿瘤部位。在本工作中,制备了宝石负载牛血清白蛋白纳米颗粒(Gem-BSANPs)并包被透明质酸(HA-Gem-BSANPs)。粒径、zeta电位、TEM和DSC分析表征了发育的NPs。Gem-BSANPs和HA-Gem-BSANPs的平均粒径、PDI和zeta电位分别为120.9±5.87 vs 144.7±5.67和28.66±1.10 vs -45.72±3.24。有趣的是,ha包被的Gem-BSANPs被发现对A549细胞系具有更高的细胞毒性,具有更好的杀伤动力学和由于CD44过表达而导致的线粒体膜损失。本研究表明,HA-Gem-BSANPs可能是通过选择性靶向肿瘤部位来提高gem治疗效果的潜在策略。
Fabrication and Evaluation of Hyaluronic Acid Coated Albumin Nanoparticles for Delivery of Gemcitabine.
Gemcitabine (Gem) is a well-known antineoplastic drug used for several solid tumors. The clinical application of gem is hampered owing to non-selectivity, short half-life, and drug resistance, which necessitate the development of a suitable novel formulation that can selectively target cancer sites. In the present work, Gem-loaded bovine serum albumin nanoparticles (Gem-BSANPs) have been prepared and coated with hyaluronic acid (HA-Gem-BSANPs). Particle size, zeta potential, TEM, and DSC analysis characterized the developed NPs. The mean particle size, PDI, and zeta potentials were observed to be 120.9 ± 5.87 vs 144.7 ± 5.67 and 28.66 ± 1.10 vs -45.72 ± 3.24, for Gem-BSANPs and HA-Gem-BSANPs, respectively. Interestingly, HA-coated Gem-BSANPs were found higher cytotoxic against A549 cell lines with better killing kinetics and mitochondrial membrane loss due to overexpression of CD44. The present work demonstrated that HA-Gem-BSANPs could be a potential strategy to improve the therapeutic efficacy of gem by selectively targeting to the tumor site.