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首页> 外文期刊>International Journal of Nanotechnology >Andrographolide, a novel bioactive phytoconstituent encapsulated in sustained release biodegradable nanoparticles
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Andrographolide, a novel bioactive phytoconstituent encapsulated in sustained release biodegradable nanoparticles

机译:穿心莲内酯,一种包裹在缓释生物可降解纳米颗粒中的新型生物活性植物成分

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摘要

Polymeric nanoparticles are advantageous in cancer therapy as they improve the physicochemical properties of drugs and consequently their behaviour in-vitro and the bioavailability of drugs. Andrographolide is a bioactive phytoconstituent widely used in the treatment of various tumours. However, the clinical efficacy by oral administration is contrasted by its biopharmaceutical properties. Hence an alternative dosage form and route of administration is investigated in the present study to enhance its therapeutic efficacy. Sustained release injectable andrographolide-loaded biodegradable poly(ε-caprolactone) (PCL) nanoparticle suspension was prepared by a solvent displacement process using poly(ethylene oxide) -poly(propylene oxide)-poly(ethylene oxide) (PEO-PPO-PEO) triblock polymeric stabiliser (Pluronic F-68/Pluronic F-127). The nanoparticles were characterised in terms of particle size, encapsulation efficiency, zeta potential, surface morphology and crystallinity. In-vitro drug release studies were carried out in presence and absence of the enzyme Candida rugose lipase in phosphate-buffered saline (PBS, pH 7.4) at 37℃ using the dialysis bag diffusion technique. The obtained suspended nanoparticles were spherical in shape with particle size of 226 ± 2 to 339 ± 5 nm and zeta potential -25.2 ± 1.6 to -27.7 ± 1.3 mV. Higher value of Q_(25hr) (cumulative percentage release at the end of 25 h) and lower values of t_(50%) and t_(80%) (time required for 50% and 80% w/w drug release) indicated the suitability of PCL nanoparticles in controlled release, which followed diffusion mechanism. The study suggested the applicability of PCL nanoparticles to improve the biopharmaceutical properties ofphytoconstituents in cancer chemotherapy.
机译:聚合纳米颗粒在癌症治疗中是有利的,因为它们改善了药物的物理化学性质,因此改善了它们的体外行为和药物的生物利用度。穿心莲内酯是一种广泛用于治疗各种肿瘤的生物活性植物成分。但是,口服给药的临床功效与其生物药理特性相反。因此,在本研究中研究了替代剂型和给药途径以增强其治疗功效。使用聚(环氧乙烷)-聚(环氧丙烷)-聚(环氧乙烷)(PEO-PPO-PEO)通过溶剂置换法制备了缓释可注射穿心莲内酯的生物可降解聚(ε-己内酯)(PCL)纳米颗粒悬浮液三嵌段聚合物稳定剂(Pluronic F-68 / Pluronic F-127)。根据粒度,包封效率,ζ电势,表面形态和结晶度表征纳米颗粒。使用透析袋扩散技术,在37℃磷酸盐缓冲液(PBS,pH 7.4)中存在和不存在念珠菌皱纹脂肪酶的条件下进行体外药物释放研究。所得的悬浮纳米颗粒为球形,粒径为226±2至339±5nm,ζ电势为-25.2±1.6至-27.7±1.3mV。 Q_(25hr)的较高值(25 h结束时的累积释放百分比)和t_(50%)和t_(80%)的较低值(50%和80%w / w药物释放所需的时间)表明PCL纳米颗粒在控释中的适应性,其遵循扩散机制。研究表明,PCL纳米颗粒可改善癌症化疗药物中植物成分的生物药物特性。

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