Literature DB >> 17523687

Specific interactions improve the loading capacity of block copolymer micelles in aqueous media.

Cristiano Giacomelli1, Vanessa Schmidt, Redouane Borsali.   

Abstract

Block copolymer micelles find application in many fields as nanocarriers, especially in drug delivery. We report herein that specific interactions between hydrophobic guest molecules and core-forming segments can significantly improve the loading capacity of polymeric micelles. High loading capacities (>100% weight/weight of polymer (w/wp)) were systematically observed for the encapsulation of probes containing weak carboxylic acid groups by micellar nanoparticles having poly[2-(dialkylamino)ethyl methacrylate] cores (i.e., particles whose cargo space exhibits antagonist weak base functions), as demonstrated by the incorporation of indomethacin (IND), ibuprofen (IBPF), and trans-3,5-bis(trifluoromethyl)cinnamic acid (F-CIN) into either poly(ethylene oxide)-b-poly[2-(diisopropylamino)ethyl methacrylate] (PEO-b-PDPA) or poly(glycerol monomethacrylate)-b-PDPA (PG2MA-b-PDPA) micelles. The esterification of IND yielding to a nonionizable IND ethyl ester derivative (IND-Et) caused an abrupt decrease in the micellar loading capacity down to 10-15% w/wp. Similar results were also obtained when IND was combined with nonionizable block copolymers such as PEO-b-polycaprolactone (PEO-b-PCL) and PEO-b-poly(glycidyl methacrylate) (PEO-b-PGMA). The existence of acid-base interactions between the solubilizate and the weak polybase block forming the micelle core was confirmed by 1H NMR measurements. However, the incorporation of high numbers of hydrophobic guest molecules inside polymeric micelles can provoke not only an increase in the hydrodynamic size (2RH) of the objects but also a substantial change in the morphology (transition from spheres to cylinders). The application of the Higuchi model showed that the probe release followed a diffusion-controlled mechanism, and diffusion coefficients (D) on the order of 10-18-10-17 cm2/s were determined for IND release from 1.0 mg/mL PEO113-b-PDPA50 + 100% w/wp IND. Probe release from micelles with weak polybase-based cores can also be triggered by changes in the solution pH.

Entities:  

Year:  2007        PMID: 17523687     DOI: 10.1021/la700337s

Source DB:  PubMed          Journal:  Langmuir        ISSN: 0743-7463            Impact factor:   3.882


  4 in total

Review 1.  Nanoparticle-mediated drug delivery for treating melanoma.

Authors:  Vaibhav Mundra; Wei Li; Ram I Mahato
Journal:  Nanomedicine (Lond)       Date:  2015-08-05       Impact factor: 5.307

2.  Fmoc-conjugated PEG-vitamin E2 micelles for tumor-targeted delivery of paclitaxel: enhanced drug-carrier interaction and loading capacity.

Authors:  Yifei Zhang; Yixian Huang; Wenchen Zhao; Jianqin Lu; Peng Zhang; Xiaolan Zhang; Jiang Li; Xiang Gao; Raman Venkataramanan; Song Li
Journal:  AAPS J       Date:  2014-09-06       Impact factor: 4.009

Review 3.  Polymeric micelles: nanocarriers for cancer-targeted drug delivery.

Authors:  Yifei Zhang; Yixian Huang; Song Li
Journal:  AAPS PharmSciTech       Date:  2014-04-04       Impact factor: 3.246

4.  Electrostatic interactions between polyglutamic acid and polylysine yields stable polyion complex micelles for deoxypodophyllotoxin delivery.

Authors:  Yutong Wang; Liping Huang; Yan Shen; Lidan Tang; Runing Sun; Di Shi; Thomas J Webster; Jiasheng Tu; Chunmeng Sun
Journal:  Int J Nanomedicine       Date:  2017-10-30
  4 in total

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