用于提高疗效的磷脂酰胆碱(PCL)强化纳米植物药物。

IF 3.8 3区 生物学 Q1 BIOLOGY EXCLI Journal Pub Date : 2023-08-18 eCollection Date: 2023-01-01 DOI:10.17179/excli2023-6345
Devesh U Kapoor, Mansi Gaur, Akshay Parihar, Bhupendra G Prajapati, Sudarshan Singh, Ravish J Patel
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引用次数: 0

摘要

从植物中提取的植物药因其潜在的治疗功效而日益得到认可。然而,由于生物利用率低、稳定性差和定向递送等难题,它们的有效性往往受到阻碍。在本研究中,我们旨在通过开发 PCL(磷脂酰胆碱)强化纳米植物药物来提高疗效,从而解决这些局限性。PCL 是一种生物相容性和可生物降解的聚合物,被用来封装植物药物,从而提高其稳定性和生物利用度。封装过程采用了纳米沉淀法,从而形成了大小和形态可控的纳米颗粒。研究人员采用了多种分析技术,包括动态光散射、扫描电子显微镜和傅立叶变换红外光谱,对 PCL 强化纳米植物药物的理化性质进行了表征。此外,还评估了 PCL 纳米颗粒中封装植物药物的释放动力学,结果表明其释放曲线具有持续性和可控性,这对延长治疗效果至关重要。在体外细胞培养模型上进行的细胞毒性研究证实了所开发的纳米植物药物的生物相容性和无毒性。此外,还进行了体内研究,以评估 PCL 强化纳米植物药物在动物模型中的疗效。结果表明,与游离植物药相比,纳米植物药的生物利用度、靶向组织分布和治疗效果均有所提高。此外,所开发的纳米植物药还能延长在血液中的循环时间,从而改善给药效果并减少给药次数。本综述强调了 PCL 强化纳米植物药物作为提高植物药物疗效的有效方法的巨大潜力。这种制剂策略可提高稳定性、生物利用度、缓释性和靶向给药性,为推动植物疗法的发展提供了大好机会。另见图表摘要(图 1)。
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Phosphatidylcholine (PCL) fortified nano-phytopharmaceuticals for improvement of therapeutic efficacy.

Phytopharmaceuticals, derived from plants, are increasingly recognized for their potential therapeutic benefits. However, their effectiveness is often hindered by challenges such as poor bioavailability, stability, and targeted delivery. In this study, we aimed to address these limitations by developing PCL (phosphatidylcholine) fortified nano-phytopharmaceuticals to enhance therapeutic efficacy. PCL, a biocompatible and biodegradable polymer, was employed to encapsulate the phytopharmaceuticals, thereby improving their stability and bioavailability. The encapsulation process utilized nanoprecipitation, resulting in the formation of nanoparticles with controlled size and morphology. Various analytical techniques were employed to characterize the physicochemical properties of PCL fortified nano-phytopharmaceuticals, including dynamic light scattering, scanning electron microscopy, and Fourier-transform infrared spectroscopy. Furthermore, the release kinetics of encapsulated phytopharmaceuticals from PCL nanoparticles were evaluated, demonstrating sustained and controlled release profiles, essential for prolonged therapeutic effects. Cytotoxicity studies conducted on in vitro cell culture models confirmed the biocompatibility and non-toxic nature of the developed nano-phytopharmaceuticals. Additionally, in vivo studies were conducted to assess the therapeutic efficacy of PCL fortified nano-phytopharmaceuticals in animal models. The results showIased improved bioavailability, targeted tissue distribution, and enhanced therapeutic effects compared to free phytopharmaceuticals. Moreover, the developed nano-phytopharmaceuticals exhibited prolonged circulation time in the bloodstream, enabling improved drug delivery and reduced dosing frequency. This review highlights the promising potential of PCL fortified nano-phytopharmaceuticals as an effective approach for enhancing the therapeutic efficacy of phytopharmaceuticals. The improved stability, bioavailability, sustained release, and targeted delivery achieved through this formulation strategy offer promising opportunities for advancing plant-based therapies. See also the Graphical abstract(Fig. 1).

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来源期刊
EXCLI Journal
EXCLI Journal BIOLOGY-
CiteScore
8.00
自引率
2.20%
发文量
65
审稿时长
6-12 weeks
期刊介绍: EXCLI Journal publishes original research reports, authoritative reviews and case reports of experimental and clinical sciences. The journal is particularly keen to keep a broad view of science and technology, and therefore welcomes papers which bridge disciplines and may not suit the narrow specialism of other journals. Although the general emphasis is on biological sciences, studies from the following fields are explicitly encouraged (alphabetical order): aging research, behavioral sciences, biochemistry, cell biology, chemistry including analytical chemistry, clinical and preclinical studies, drug development, environmental health, ergonomics, forensic medicine, genetics, hepatology and gastroenterology, immunology, neurosciences, occupational medicine, oncology and cancer research, pharmacology, proteomics, psychiatric research, psychology, systems biology, toxicology
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