Effect of Formulation and Processing Parameters on the Size of mPEG-b-p(HPMA-Bz) Polymeric Micelles
Open Access
- 12 November 2018
- journal article
- research article
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 34 (50) , 15495-15506
Abstract
Micelles composed of block copolymers of poly(ethylene glycol)-b-poly(N-2-benzoyloxypropyl methacrylamide) (mPEG-b-p(HPMA-Bz)) have shown great promise as drug delivery carriers due to their excellent stability and high loading capacity. In the present study, parameters influencing micelle size were investigated to tailor sizes in the range of 25 to 100 nm. Micelles were prepared by a nanoprecipitation method and their size was modulated by the block copolymer properties such as molecular weight, their hydrophilic to hydrophobic ratio, homopolymer content, as well as formulation and processing parameters. It was shown that the micelles have a core-shell structure using a combination of dynamic light scattering and transmission electron microscopy analysis. By varying the degree of polymerization of the hydrophobic block (NB) between 68 and 10, at a fixed hydrophilic block mPEG5K (NA=114), it was shown that the hydrophobic core of the micelle was collapsed following the power law of (NB×Nagg)1/3. Further, the calculated brush height was similar for all the micelles examined (10 nm), indicating that crew-cut micelles were made. Both addition of homopolymer and preparation of micelles at lower concentrations or lower rates of addition of the organic solvent to the aqueous phase increased the size of micelles due to partitioning of the hydrophobic homopolymer chains to the core of the micelles and lower nucleation rates, respectively. Furthermore, it was shown that by using different solvents, the size of the micelles substantially changed. The use of acetone, acetonitrile, ethanol, THF and dioxane, resulted in micelles in the size range from 45 to 60 nm after removal of the organic solvents. The use of DMF and DMSO led to markedly larger sizes of 75 and 180 nm respectively. In conclusion, the results show that by modulating polymer properties and processing conditions, micelles with tailorable sizes can be obtained.Keywords
Funding Information
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (13312)
This publication has 72 references indexed in Scilit:
- Bridging Bio–Nano Science and Cancer NanomedicineACS Nano, 2017
- Overcoming the Road Blocks: Advancement of Block Copolymer Micelles for Cancer Therapy in the ClinicMolecular Pharmaceutics, 2017
- Polymeric mixed micelles as nanomedicines: Achievements and perspectivesEuropean Journal of Pharmaceutics and Biopharmaceutics, 2017
- Challenges and strategies in anti-cancer nanomedicine development: An industry perspectiveAdvanced Drug Delivery Reviews, 2017
- Nanomedicines for advanced cancer treatments: Transitioning towards responsive systemsInternational Journal of Pharmaceutics, 2016
- Noninvasive Imaging of Nanomedicines and Nanotheranostics: Principles, Progress, and ProspectsChemical Reviews, 2015
- Progress of drug-loaded polymeric micelles into clinical studiesJournal of Controlled Release, 2014
- Polymer therapeutics-prospects for 21st century: The end of the beginningAdvanced Drug Delivery Reviews, 2013
- Biodegradable polymeric micelles for targeted and controlled anticancer drug delivery: Promises, progress and prospectsNano Today, 2012
- Block copolymer micelles for delivery of cancer therapy: Transport at the whole body, tissue and cellular levelsJournal of Controlled Release, 2009