自纳米乳化给药系统(SNEDDS)作为BCS III类药物通透性调节途径的纳米载体框架。

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Amulya Jindal, Pankaj Kumar Sharma, Anoop Kumar
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引用次数: 0

摘要

本文综述了自纳米乳化给药系统(SNEDDS)作为一种有效的纳米载体框架,用于BCS iii类药物的渗透性调节方法(PMA)及其面临的挑战。目前的审查更新了SNEDDS研究的最新趋势,其中它被用作PMA的货物载体和挑战。患者的依从性、给药的便利性和无创方式是口服给药的重要方面。然而,水溶解度低和渗透性受损是导致药物吸收不良的两个突出挑战。SNEDDS是一种双纳米载体系统,通过离子配对、磷脂复合物、表面活性剂-药物相互作用、负载非电离性、游离药物碱等方式实现PMA的纳米分散。这些pma被嵌入到SNEDDS的脂质相中产生纳米尺寸,由于其三元组分,通过胶束/增溶机制增强纳米分散性。综述重点介绍了用于增强BCS III类生物利用度的不同pma。它涵盖了sndds负载PMA中使用的赋形剂,BCS iii类药物水溶性药物的疏水转化策略。SNEDDS作为pma的纳米货物系统,显著改变了BCS iii类药物的生物利用度。SNEDDS是一种油、表面活性剂和助表面活性剂的各向同性混合物,可提供多点接触PMA负载,并在水介质中产生纳米分散体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-nanoemulsifying drug delivery system (SNEDDS) as nano-carrier framework for permeability modulating approaches of BCS class III drug.

The purpose of this review is to focus on the Self-Nanoemulsifying Drug Delivery System (SNEDDS) as an effective nanocarrier framework for permeability modulating approaches (PMA) of BCS class-III drugs and its challenges. Present review updates the recent trends in the SNEDDS research where it was employed as a cargo carrier for PMA and challenges. Patient compliance, ease of administration and non-invasiveness mode are non-trivial aspects in the oral administration of drugs. However, low aqueous solubility and impaired permeability are two prominent challenges resulting poor absorption of a drug. SNEDDS emerged as a dual nano-carrier system to enable nanodispersion of PMA via e.g. ion-pairing, phospholipid-complex, surfactant-drug interaction, loading of non-ionizable, free drug bases etc. These PMAs are embedded within the lipid phase of SNEDDS to produce nanosizing, enhancing nano-dispersibility via micellization/solubilization mechanism owing to its ternary components. Review highlights different PMAs employed in bioavailability enhancement of BCS class-III. It covers excipients employed in SNEDDS-loaded PMA, strategies for the hydrophobic transformation of water-soluble drugs for BCS class-III drugs. SNEDDS as a nano-cargo system for PMAs significantly modifies the bioavailability of BCS class-III drugs. SNEDDS is an isotropic-mixture of oil, surfactant:co-surfactant offers multipoint access to PMA loading and produces nano-dispersion in aqueous-medium.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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