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相关概念视频

Bioavailability Enhancement: Drug Permeability Enhancement01:27

Bioavailability Enhancement: Drug Permeability Enhancement

After oral administration, poor permeability often limits the rate at which drugs are absorbed through the intestinal epithelium. Enhancing drug permeability is crucial for effective therapy, and several strategies have been developed to overcome this challenge.One effective strategy involves the use of lipid-based formulations. These formulations enhance dissolution and solubility, targeting physiological mechanisms to increase drug absorption. This includes stimulating bile salt secretion,...
Bioavailability Enhancement: Drug Stability Enhancement and GI Retention01:05

Bioavailability Enhancement: Drug Stability Enhancement and GI Retention

Improving a drug's stability in the gastrointestinal (GI) tract is paramount for enhancing its bioavailability and therapeutic effectiveness. Various strategies are employed to protect the drug from the harsh gastric milieu and to ensure its release and absorption at the desired site within the GI tract.Polymer coatings are one such method used to shield drugs from the stomach's acidic environment. By preventing premature drug release, these coatings improve the bioavailability of unstable...
Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence01:27

Pharmaceutical Alternatives: Polymorphic Form-Related and Particle Size-Related Therapeutic Nonequivalence

Changes in polymorphic forms can significantly influence the bioavailability of poorly soluble drugs. Although the FDA defines pharmaceutical equivalence based on having the same active ingredient, dosage form, and route of administration, it does not automatically disqualify products with different polymorphic forms. This means two products with different polymorphs can still be deemed pharmaceutically equivalent. However, polymorphic differences can affect properties like wettability,...
Modified-Release Drug Delivery Systems: Rate-Programmed II01:19

Modified-Release Drug Delivery Systems: Rate-Programmed II

Rate-programmed drug delivery systems release drugs in a controlled manner to maintain therapeutic levels. Three main designs include reservoir, matrix, and hybrid systems.Reservoir systems consist of a drug core enclosed within a membrane that controls drug release. In non-swelling reservoir systems, polymers like ethyl cellulose or polymethacrylates are used. These do not hydrate in aqueous media and control release through membrane thickness, porosity, or insolubility. This type includes...
Site-Targeted Drug Delivery Systems: Polymeric Carriers01:24

Site-Targeted Drug Delivery Systems: Polymeric Carriers

Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
Bioplastics01:27

Bioplastics

Bioplastics derived from microbial processes present a sustainable alternative to conventional petroleum-based plastics. Among these, polyhydroxyalkanoates (PHAs), particularly polyhydroxybutyrates (PHBs), have emerged as prominent candidates due to their biodegradability and biocompatibility. These polymers are synthesized by a variety of bacteria, such as Cupriavidus necator and Pseudomonas putida, which naturally accumulate PHAs as intracellular carbon and energy reserves, especially under...

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Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
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可生物降解的Zwitterionic聚合物作为药物输送中的PEG替代品

Ziwen Zhang1, Haotian Sun1, Justin Giannino2

  • 1Department of Chemical and Biological Engineering, University at Buffalo, the State University of New York, Buffalo, NY 14260.

Journal of polymer science (2020)
|September 9, 2024
PubMed
概括
此摘要是机器生成的。

可生物降解的基聚合物 (ZPs) 由于其生物相容性和降低免疫性,为聚乙烯糖醇 (PEG) 提供了一个有前途的替代品. 这些先进材料显示出改善药物输送系统的潜力,而不会产生长期副作用.

关键词:
这是一种PEG替代品.可生物降解的聚合物聚合物药物输送是药物输送的过程.提供蛋白质的蛋白质输送.这是一种zwitterionic聚合物.

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科学领域:

  • 生物材料科学 生物材料科学
  • 聚合物化学 聚合物化学
  • 药物输送系统 药物输送系统

背景情况:

  • 聚乙烯甘醇 (PEG) 在生物医学中广泛使用,但患有免疫性,限制治疗疗效.
  • 化治疗药物可以引起免疫反应,限制其临床应用.
  • 对于先进的生物医学应用,需要具有免疫性降低的生物相容聚合物.

研究的目的:

  • 提供可生物降解的紫聚合物 (ZPs) 作为PEG.的替代品的全面审查.
  • 讨论可生物降解ZPs的结构设计和合成策略.
  • 突出生物降解ZPs在药物输送中的应用.

主要方法:

  • 对生物降解ZPs的最新科学文献进行系统审查.
  • 对结构设计和合成方法的分析,用于将可生物降解的聚合物与zwitterions集成.
  • 评估ZP在提供小分子药物和蛋白质方面的应用.

主要成果:

  • 可生物降解的ZPs具有出色的水溶性和免疫性惰性.
  • 这些聚合物提供了有利的生物医学特性,没有显著的长期副作用.
  • 已开发出各种可生物降解ZPs的结构设计和合成方法.

结论:

  • 生物降解ZPs代表了与传统的基于PEG的材料相比的重大进步.
  • 它们的可调节性质和生物相容性使得它们非常适合用于各种药物输送应用.
  • 对生物降解ZPs的进一步研究有望改善治疗效果并减少不良影响.