• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

采用纳米沉淀技术制备高载药量的草药亲水性药物聚合物纳米粒:一种质量源于设计的方法

Development of polymeric nanoparticles with highly entrapped herbal hydrophilic drug using nanoprecipitation technique: an approach of quality by design.

作者信息

Vuddanda Parameswara Rao, Mishra Amit, Singh Sanjay Kumar, Singh Sanjay

机构信息

Department of Pharmaceutics, Indian Institute of Technology (Banaras Hindu University) , Varanasi, Uttar Pradesh , India.

出版信息

Pharm Dev Technol. 2015;20(5):579-87. doi: 10.3109/10837450.2014.908302. Epub 2014 May 15.

DOI:10.3109/10837450.2014.908302
PMID:24831535
Abstract

The intention of this study is to achieve higher entrapment efficiency (EE) of berberine chloride (selected hydrophilic drug) using nanoprecipitation technique. The solubility of drug was studied in various pH buffers (1.2-7.2) for selection of aqueous phase and stabilizer. Quality by design (QbD)-based 3(2) factorial design were employed for optimization of formulation variables; drug to polymer ratio (X1) and surfactant concentration (X2) on entrapment efficiency (EE), particle size (PS) and polydispersity index (PDI) of the nanoparticles. The nanoparticles were subjected to solid state analysis, in vitro drug release and stability study. The aqueous phase and stabilizer selected for the formulations were pH 4.5 phthalate buffer and surfactant F-68, respectively. The formulation (F-6) containing drug to polymer ratio (1:3) and stabilizer (F-68) concentration of 50 mM exhibited best EE (82.12%), PS (196.71 nm), PDI (0.153). The various solid state characterizations assured that entrapped drug is amorphous and nanoparticles are fairly spherical in shape. In vitro drug release of the F-6 exhibited sustained release with non-Fickian diffusion and stable at storage condition. This work illustrates that the proper selection of aqueous phase and optimization of formulation variables could be helpful in improving the EE of hydrophilic drugs by nanoprecipitation technique.

摘要

本研究旨在利用纳米沉淀技术提高盐酸小檗碱(所选亲水性药物)的包封率(EE)。研究了药物在各种pH缓冲液(1.2 - 7.2)中的溶解度,以选择水相和稳定剂。采用基于质量源于设计(QbD)的3(2)析因设计来优化配方变量;药物与聚合物比例(X1)和表面活性剂浓度(X2)对纳米颗粒的包封率(EE)、粒径(PS)和多分散指数(PDI)的影响。对纳米颗粒进行了固态分析、体外药物释放和稳定性研究。为配方选择的水相和稳定剂分别是pH 4.5的邻苯二甲酸盐缓冲液和表面活性剂F - 68。含有药物与聚合物比例为(1:3)和稳定剂(F-68)浓度为50 mM的配方(F-6)表现出最佳的包封率(82.12%)、粒径(196.71 nm)和多分散指数(0.153)。各种固态表征确保了包封的药物为无定形,且纳米颗粒形状相当球形。F-6的体外药物释放呈现出非菲克扩散的缓释特性,并且在储存条件下稳定。这项工作表明,水相的适当选择和配方变量的优化有助于通过纳米沉淀技术提高亲水性药物的包封率。

相似文献

1
Development of polymeric nanoparticles with highly entrapped herbal hydrophilic drug using nanoprecipitation technique: an approach of quality by design.采用纳米沉淀技术制备高载药量的草药亲水性药物聚合物纳米粒:一种质量源于设计的方法
Pharm Dev Technol. 2015;20(5):579-87. doi: 10.3109/10837450.2014.908302. Epub 2014 May 15.
2
Exploration of statistical experimental design to improve entrapment efficiency of acyclovir in poly (d, l) lactide nanoparticles.探索统计实验设计以提高聚(D,L)丙交酯纳米粒中阿昔洛韦的包封效率。
Pharm Dev Technol. 2014 Mar;19(2):200-12. doi: 10.3109/10837450.2013.769566. Epub 2013 Feb 25.
3
Quality by design approach to understand the process of optimization of iloperidone nanostructured lipid carriers for oral bioavailability enhancement.采用质量源于设计的方法来理解用于提高口服生物利用度的伊潘立酮纳米结构脂质载体的优化过程。
Pharm Dev Technol. 2015 May;20(3):320-9. doi: 10.3109/10837450.2013.867445. Epub 2013 Dec 13.
4
DoE based Olanzapine loaded poly-caprolactone nanoparticles decreases extrapyramidal effects in rodent model.基于实验设计的奥氮平载入聚己内酯纳米粒可减少啮齿类动物模型的锥体外系副作用。
Int J Pharm. 2018 Apr 25;541(1-2):198-205. doi: 10.1016/j.ijpharm.2018.02.010. Epub 2018 Feb 21.
5
Preparation and characterization of nanoparticles containing an atypical antipsychotic agent.含非典型抗精神病药物纳米颗粒的制备与表征
Nanomedicine (Lond). 2007 Apr;2(2):233-40. doi: 10.2217/17435889.2.2.233.
6
Application of quality by design approach for intranasal delivery of rivastigmine loaded solid lipid nanoparticles: Effect on formulation and characterization parameters.质量源于设计方法在载有卡巴拉汀的固体脂质纳米粒鼻腔给药中的应用:对制剂和表征参数的影响。
Eur J Pharm Sci. 2015 Oct 12;78:54-66. doi: 10.1016/j.ejps.2015.07.002. Epub 2015 Jul 2.
7
Optimization and evaluation of bioactive drug-loaded polymeric nanoparticles for drug delivery.用于药物递送的载药高分子纳米粒的优化与评价。
Int J Biol Macromol. 2015;78:173-9. doi: 10.1016/j.ijbiomac.2015.03.070. Epub 2015 Apr 13.
8
Solid self microemulsification of Atorvastatin using hydrophilic carriers: a design.使用亲水性载体的阿托伐他汀固体自微乳化:一种设计
Drug Dev Ind Pharm. 2015;41(7):1213-22. doi: 10.3109/03639045.2014.938655. Epub 2014 Jul 14.
9
Design and optimization of NSAID loaded nanoparticles.非甾体抗炎药负载纳米颗粒的设计与优化。
Pak J Pharm Sci. 2007 Apr;20(2):157-62.
10
Terbinafine-loaded branched PLGA-based cationic nanoparticles with modifiable properties.载有特比萘芬的具有可修饰性能的支化 PLGA 基阳离子纳米粒。
Pharm Dev Technol. 2019 Dec;24(10):1308-1316. doi: 10.1080/10837450.2019.1667387. Epub 2019 Sep 25.

引用本文的文献

1
Expatiating the Pharmacological and Nanotechnological Aspects of the Alkaloidal Drug Berberine: Current and Future Trends.阐述生物碱药物小檗碱的药理学和纳米技术方面:现状和未来趋势。
Molecules. 2022 Jun 9;27(12):3705. doi: 10.3390/molecules27123705.
2
Exploring Various Techniques for the Chemical and Biological Synthesis of Polymeric Nanoparticles.探索用于聚合物纳米颗粒化学和生物合成的各种技术。
Nanomaterials (Basel). 2022 Feb 8;12(3):576. doi: 10.3390/nano12030576.
3
Development, optimization, and evaluation of PEGylated brucine-loaded PLGA nanoparticles.
聚乙二醇化蝙蝠葛堿载 PLGA 纳米粒的制备、优化及评价。
Drug Deliv. 2020 Dec;27(1):1134-1146. doi: 10.1080/10717544.2020.1797237.
4
Hydrogel Formulation for Intra-Articular Application of Diclofenac Sodium-Loaded Polymeric Nanoparticles.用于关节腔内应用载有双氯芬酸钠的聚合物纳米颗粒的水凝胶制剂。
Turk J Pharm Sci. 2017 Apr;14(1):56-64. doi: 10.4274/tjps.84803. Epub 2017 Apr 15.
5
Developments in drug delivery of bioactive alkaloids derived from traditional Chinese medicine.中药生物活性生物碱药物传递系统的研究进展。
Drug Deliv. 2018 Nov;25(1):398-416. doi: 10.1080/10717544.2018.1431980.