• 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

用于制备微球的新型可生物吸收和生物消除的表面活性剂。

Novel bioresorbable and bioeliminable surfactants for microsphere preparation.

作者信息

Bouillot P, Babak V, Dellacherie E

机构信息

Laboratoire de Chimie Physique Macromoleculaire, ENSIC, Nancy, France.

出版信息

Pharm Res. 1999 Jan;16(1):148-54. doi: 10.1023/a:1018895417915.

DOI:10.1023/a:1018895417915
PMID:9950294
Abstract

PURPOSE

The objective of this work is to prepare microspheres by the emulsion-solvent evaporation process using MPOE-PLA copolymers as the matrix material and/or the surfactant. This preparation was studied in order to avoid the use of PVA as the surfactant in the process.

METHODS

Two series of MPOE-PLA copolymers were synthesised. The first, with a long and constant length PLA chain (45,000 g.mol(-1), was used as the matrix material, the second, with short PLA chains (< or = 2.200 g.mol(-1)), and different HLB as the surfactant. Microspheres were prepared by the "simple" and "double" emulsion methods. The steric stabilization effect of the copolymers was investigated using confocal microscopy and X-ray photoelectron spectroscopy (XPS).

RESULTS

Confocal microscopy and XPS analysis showed that the microspheres prepared using MPOE5K-PLA0.5K as the surfactant and MPOE-PLA45K copolymers as the matrix material had an MPOE coating present at the microsphere surface. This hydrophilic layer ensures steric stabilization of the particles.

CONCLUSIONS

MPOE-PLA copolymers can be used for the preparation of particles instead of PVA and their use can be extended whenever a biocompatible and bioeliminable surfactant is required for biological or medical applications.

摘要

目的

本研究旨在以MPOE-PLA共聚物作为基质材料和/或表面活性剂,通过乳液-溶剂蒸发法制备微球。进行该制备研究是为了避免在该过程中使用聚乙烯醇(PVA)作为表面活性剂。

方法

合成了两个系列的MPOE-PLA共聚物。第一个系列具有长且恒定长度的PLA链(45,000 g·mol⁻¹),用作基质材料;第二个系列具有短PLA链(≤2,200 g·mol⁻¹),且具有不同的亲水亲油平衡值(HLB),用作表面活性剂。通过“简单”和“双重”乳液法制备微球。使用共聚焦显微镜和X射线光电子能谱(XPS)研究共聚物的空间稳定作用。

结果

共聚焦显微镜和XPS分析表明,以MPOE5K-PLA0.5K作为表面活性剂、MPOE-PLA45K共聚物作为基质材料制备的微球,其表面存在MPOE涂层。该亲水层确保了颗粒的空间稳定性。

结论

MPOE-PLA共聚物可用于替代PVA制备颗粒,并且只要生物或医学应用需要生物相容性和可生物降解的表面活性剂,其应用就可以扩展。

相似文献

1
Novel bioresorbable and bioeliminable surfactants for microsphere preparation.用于制备微球的新型可生物吸收和生物消除的表面活性剂。
Pharm Res. 1999 Jan;16(1):148-54. doi: 10.1023/a:1018895417915.
2
Protein encapsulation in biodegradable amphiphilic microspheres.蛋白质包裹于可生物降解的两亲性微球中。
Int J Pharm. 1999 Apr 30;181(2):159-72. doi: 10.1016/s0378-5173(99)00023-x.
3
Surfactive water-soluble copolymers for the preparation of controlled surface nanoparticles by double emulsion/solvent evaporation.用于通过双乳液/溶剂蒸发制备可控表面纳米颗粒的表面活性水溶性共聚物。
Colloids Surf B Biointerfaces. 2006 Aug 1;51(1):86-92. doi: 10.1016/j.colsurfb.2006.04.003. Epub 2006 May 2.
4
Development of poly (lactic acid) microspheres and their potential application in Pickering emulsions stabilization.聚乳酸微球的制备及其在 Pickering 乳液稳定化中的潜在应用。
Int J Biol Macromol. 2018 Mar;108:105-111. doi: 10.1016/j.ijbiomac.2017.11.079. Epub 2017 Nov 13.
5
Morphology control of polylactide microspheres enclosing irinotecan hydrochloride with polylactide based polymer surfactant for reduction of initial burst.使用基于聚乳酸的聚合物表面活性剂控制包裹盐酸伊立替康的聚乳酸微球的形态以减少初始突释
Int J Pharm. 2007 Feb 7;330(1-2):32-6. doi: 10.1016/j.ijpharm.2006.08.035. Epub 2006 Aug 30.
6
Surface characterization of poly(alpha-hydroxy acid) microspheres prepared by a solvent evaporation/extraction process.通过溶剂蒸发/萃取法制备的聚(α-羟基酸)微球的表面表征
Biomaterials. 1997 Jan;18(2):125-36. doi: 10.1016/s0142-9612(96)00102-0.
7
Transport of PLA-PEG particles across the nasal mucosa: effect of particle size and PEG coating density.聚乳酸-聚乙二醇颗粒经鼻黏膜的转运:粒径和聚乙二醇包衣密度的影响
J Control Release. 2004 Aug 11;98(2):231-44. doi: 10.1016/j.jconrel.2004.04.026.
8
Microcosmic mechanisms for protein incomplete release and stability of various amphiphilic mPEG-PLA microspheres.各种两亲性 mPEG-PLA 微球的蛋白质不完全释放和稳定性的微观机制。
Langmuir. 2012 Oct 2;28(39):13984-92. doi: 10.1021/la3017112. Epub 2012 Sep 17.
9
Controlled release of the fibronectin central cell binding domain from polymeric microspheres.纤连蛋白中央细胞结合结构域从聚合物微球中的控释。
J Control Release. 2004 Mar 24;95(3):557-66. doi: 10.1016/j.jconrel.2003.12.016.
10
Biocompatible and pH-Responsive Colloidal Surfactants with Tunable Shape for Controlled Interfacial Curvature.具有可调形状的生物相容和 pH 响应胶体表面活性剂,用于控制界面曲率。
Angew Chem Int Ed Engl. 2020 Jun 8;59(24):9365-9369. doi: 10.1002/anie.202001588. Epub 2020 Apr 6.

引用本文的文献

1
Amphiphilic Acrylic Nanoparticles Containing the Poloxamer Star Bayfit® 10WF15 as Ophthalmic Drug Carriers.含有泊洛沙姆星型Bayfit® 10WF15的两亲性丙烯酸纳米颗粒作为眼科药物载体
Polymers (Basel). 2019 Jul 19;11(7):1213. doi: 10.3390/polym11071213.
2
Structural analysis of microparticles by confocal laser scanning microscopy.通过共聚焦激光扫描显微镜对微粒进行结构分析。
AAPS PharmSciTech. 2000 Jun 23;1(3):E17. doi: 10.1208/pt010317.

本文引用的文献

1
Carcinogenic studies on water-soluble and insoluble macromolecules.
AMA Arch Pathol. 1959 Jun;67(6):589-617.
2
The immune response to a model antigen associated with PLG microparticles prepared using different surfactants.对使用不同表面活性剂制备的与纤溶酶原(PLG)微粒相关的模型抗原的免疫反应。
Vaccine. 1997 Dec;15(17-18):1888-97. doi: 10.1016/s0264-410x(97)00134-5.
3
The Adsorption of Poly(vinyl alcohol) to Biodegradable Microparticles Studied by X-Ray Photoelectron Spectroscopy (XPS).用X射线光电子能谱(XPS)研究聚乙烯醇在可生物降解微粒上的吸附。
J Colloid Interface Sci. 1997 Jan 15;185(2):538-47. doi: 10.1006/jcis.1996.4637.
4
Degradation behaviour of block copolymers containing poly(lactic-glycolic acid) and poly(ethylene glycol) segments.含有聚乳酸-乙醇酸和聚乙二醇链段的嵌段共聚物的降解行为。
Biomaterials. 1996 Aug;17(16):1583-90. doi: 10.1016/0142-9612(95)00323-1.
5
Rifampicin carrying poly (D,L-lactide)/poly(ethylene glycol) microspheres: loading and release.载利福平的聚(D,L-丙交酯)/聚乙二醇微球:负载与释放
Artif Organs. 1996 Jul;20(7):743-51. doi: 10.1111/j.1525-1594.1996.tb04535.x.
6
Controlled delivery systems for proteins using polyanhydride microspheres.
Pharm Res. 1993 Apr;10(4):487-96. doi: 10.1023/a:1018929531410.
7
Surface modification of poly(lactide-co-glycolide) nanospheres by biodegradable poly(lactide)-poly(ethylene glycol) copolymers.可生物降解的聚乳酸-聚乙二醇共聚物对聚(丙交酯-乙交酯)纳米球的表面改性
Pharm Res. 1994 Dec;11(12):1800-8. doi: 10.1023/a:1018931820564.
8
Comparison of body distribution of poly(vinyl alcohol) with other water-soluble polymers after intravenous administration.
J Pharm Pharmacol. 1995 Jun;47(6):479-86. doi: 10.1111/j.2042-7158.1995.tb05835.x.
9
Stealth Me.PEG-PLA nanoparticles avoid uptake by the mononuclear phagocytes system.隐形“我”。聚乙二醇-聚乳酸纳米粒可避免被单核吞噬细胞系统摄取。
J Pharm Sci. 1995 Apr;84(4):493-8. doi: 10.1002/jps.2600840420.
10
Histologic comparison of polylactic and polyglycolic acid sutures.聚乳酸和聚乙醇酸缝线的组织学比较
Oral Surg Oral Med Oral Pathol. 1971 Jul;32(1):165-73. doi: 10.1016/0030-4220(71)90265-9.