利用设计质量范式对辛伐他汀富含生物活性成膜喷雾剂进行综合开发研究:改善伤口愈合的前瞻性策略。

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2024-11-01 Epub Date: 2024-07-29 DOI:10.1080/1061186X.2024.2382405
Vrushali N Patel, Heta V Patel, Kashish Agrawal, Ishika Soni, Pranav Shah, Shubhada V Mangrulkar, Milind J Umekar, Manisha S Lalan
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引用次数: 0

摘要

在伤口愈合过程中使用外用抗菌药面临着耐药性风险和对局部组织的毒性等挑战。辛伐他汀(SIM)是一种可降低心血管事件风险的降血脂药,其在伤口愈合中的多效应可被重新利用。利用壳聚糖、胶原蛋白和透明质酸设计了一种基于生物活性生物粘附聚合物的辛伐他汀成膜喷雾剂(FFS)配方,并采用 DoE 方法对其进行了优化。优化后的配方具有中等粘度(12.5 ± 0.3 cP)、快速成膜(231 ± 5.6 s)、柔韧性、拉伸强度和持续药物释放(T80 - 80% 药物释放时间 - 9.05 ± 0.7 h)。扫描电子显微镜(SEM)证实了药物在复合聚合物基质中的均匀分散。SIM FFS 对革兰氏阳性菌和革兰氏阴性菌具有抗菌活性。小鼠体内切除伤口模型研究证实了生物活性聚合物的有益作用,与标准抗菌制剂相比,SIM FFS 在伤口收缩和闭合、组织重塑和重新上皮方面具有显著功效。细胞因子 TNF-α、IL-6 下调,IL-10 上调。生化指标、羟脯氨酸、己胺和组织病理学与观察到的伤口收缩一致。这是将 SIM 重新用于伤口愈合的一种新剂型的探索性努力,凸显了其作为传统外用抗菌剂替代品的潜力。
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Comprehensive developmental investigation on simvastatin enriched bioactive film forming spray using the quality by design paradigm: a prospective strategy for improved wound healing.

The use of topical antimicrobials in wound healing presents challenges like risk of drug resistance and toxicity to local tissue. Simvastatin (SIM), a lipid-lowering agent which reduces the risk of cardiovascular events, is repurposed for its pleiotropic effect in wound healing. A bioactive bioadhesive polymer-based film forming spray (FFS) formulation of SIM was designed using chitosan, collagen, hyaluronic acid and optimised by employing the DoE approach. Optimised formulation demonstrated moderate viscosity (12.5 ± 0.3 cP), rapid film formation (231 ± 5.6 s), flexibility, tensile strength and sustained drug release (T80 - time for 80% drug release - 9.05 ± 0.7 h). Scanning electron microscopy (SEM) verified uniformly dispersed drug within the composite polymer matrix. SIM FFS demonstrated antimicrobial activity against gram positive and gram negative bacteria. In vivo excision wound model studies in mice affirmed the beneficent role of bioactive polymers and the efficacy of SIM FFS in wound contraction and closure, tissue remodelling and re-epithelization in comparison to standard antimicrobial preparation. Cytokines TNF- alpha, IL-6 were downregulated and IL-10 was upregulated. Biochemical markers; hydroxyproline, hexosamine and histopathology were consistent with wound contraction observed. This is an exploratory effort in repurposing SIM for wound healing in a novel dosage form, underscoring its potential as an alternative to conventional topical antimicrobials.

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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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