Advances in nano-preparations for improving tetrandrine solubility and bioavailability

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL Archiv der Pharmazie Pub Date : 2024-06-20 DOI:10.1002/ardp.202400274
Jie Ling, Jingping Wu, Yuening Cao, Tingting Zhang, Xiujun Cao, Xian Ge, Yilan Liu, Maolin Wang, Bo Ren, Jun Lu
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Abstract

Tetrandrine (TET) is a natural bis-benzylisoquinoline alkaloid isolated from Stephania species with a wide range of biological and pharmacologic activities; it mainly serves as an anti-inflammatory agent or antitumor adjuvant in clinical applications. However, limitations such as prominent hydrophobicity, severe off-target toxicity, and low absorption result in suboptimal therapeutic outcomes preventing its widespread adoption. Nanoparticles have proven to be efficient devices for targeted drug delivery since drug-carrying nanoparticles can be passively transported to the tumor site by the enhanced permeability and retention (EPR) effects, thus securing a niche in cancer therapies. Great progress has been made in nanocarrier construction for TET delivery due to their outstanding advantages such as increased water-solubility, improved biodistribution and blood circulation, reduced off-target irritation, and combinational therapy. Herein, we systematically reviewed the latest advancements in TET-loaded nanoparticles and their respective features with the expectation of providing perspective and guidelines for future research and potential applications of TET.

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纳米制剂在提高四氢化萘溶解度和生物利用度方面的进展
四氢化苦参碱(TET)是一种天然的双苄基异喹啉生物碱,从菊科植物中分离出来,具有广泛的生物和药理活性;在临床应用中主要用作抗炎剂或抗肿瘤辅助剂。然而,由于疏水性突出、脱靶毒性严重、吸收率低等局限性,导致其治疗效果不理想,无法得到广泛应用。纳米粒子已被证明是高效的靶向给药装置,因为载药纳米粒子可以通过增强的渗透性和滞留性(EPR)效应被动地输送到肿瘤部位,从而在癌症疗法中占据一席之地。由于纳米载体具有增加水溶性、改善生物分布和血液循环、减少脱靶刺激和联合治疗等突出优势,用于 TET 给药的纳米载体构建取得了长足进展。在此,我们系统回顾了 TET 载体纳米颗粒的最新进展及其各自特点,希望能为 TET 的未来研究和潜在应用提供视角和指导。
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来源期刊
Archiv der Pharmazie
Archiv der Pharmazie 医学-化学综合
CiteScore
7.90
自引率
5.90%
发文量
176
审稿时长
3.0 months
期刊介绍: Archiv der Pharmazie - Chemistry in Life Sciences is an international journal devoted to research and development in all fields of pharmaceutical and medicinal chemistry. Emphasis is put on papers combining synthetic organic chemistry, structural biology, molecular modelling, bioorganic chemistry, natural products chemistry, biochemistry or analytical methods with pharmaceutical or medicinal aspects such as biological activity. The focus of this journal is put on original research papers, but other scientifically valuable contributions (e.g. reviews, minireviews, highlights, symposia contributions, discussions, and essays) are also welcome.
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