Drug-Loaded Polymer Colloidal Systems in Nanomedicine III

A special issue of Polymers (ISSN 2073-4360). This special issue belongs to the section "Polymer Networks".

Deadline for manuscript submissions: 30 June 2024 | Viewed by 390

Special Issue Editor

Special Issue Information

Dear Colleagues,

Further to the success of the Special Issue of Polymers “Polymeric Colloidal Systems in Nanomedicine”, I am delighted to reopen this Special Issue, now entitled “Drug-Loaded Polymer Colloidal Systems in Nanomedicine III”.

This Special Issue will integrate fundamental research with the practical application of colloidal systems in the field of nanomedicine. Of practical interest are the submicronic drug-loaded colloidal systems, such as micelles, polymersomes, nanogels, liposomes, nanocapsules, nanoparticles, nanoemulsions, etc. Another domain of interest is that of functionalized colloidal systems with specific ligands for active targeted drug delivery.

The authors will try to explain the correlations between the molecular characteristics of the starting copolymers and their colloidal characteristics, as well as the encapsulation efficiency and/or the drug release kinetics. In vitro biological analyses are welcome, but not mandatory. Regular research articles and reviews will be accepted for publication in this Special Issue.

Prof. Dr. Leonard-Ionut Atanase
Guest Editor

Manuscript Submission Information

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Keywords

  • polymeric colloids
  • micelles
  • nanogels
  • liposomes
  • nanoparticles
  • drug delivery

Published Papers (1 paper)

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12 pages, 3561 KiB  
Article
Colloidal and Biological Characterization of Dual Drug-Loaded Smart Micellar Systems
by Hildegard Herman, Delia M. Rata, Anca N. Cadinoiu, Leonard I. Atanase and Anca Hermenean
Polymers 2024, 16(9), 1189; https://doi.org/10.3390/polym16091189 - 24 Apr 2024
Viewed by 203
Abstract
Smart polymeric micelles (PMs) are of great interest in drug delivery owing to their low critical micellar concentration and sizes. In the present study, two different pH-sensitive poly(2-vinyl pyridine)-b-poly(ethylene oxide) (P2VP-b-PEO) copolymer samples were used for the encapsulation of paclitaxel (PTX), ursolic acid [...] Read more.
Smart polymeric micelles (PMs) are of great interest in drug delivery owing to their low critical micellar concentration and sizes. In the present study, two different pH-sensitive poly(2-vinyl pyridine)-b-poly(ethylene oxide) (P2VP-b-PEO) copolymer samples were used for the encapsulation of paclitaxel (PTX), ursolic acid (UA), and dual loading of PTX and UA. Based on the molecular features of copolymers, spherical PMs with sizes of around 35 nm and 140 nm were obtained by dialysis for P2VP55-b-PEO284 and P2VP274-b-PEO1406 samples, respectively. The micellar sizes increased after loading of both drugs. Moreover, drug encapsulation and loading efficiencies varied from 53 to 94% and from 3.2 to 18.7% as a function of the copolymer/drug ratio, molar mass of copolymer sample, and drug type. By FT-IR spectroscopy, it was possible to demonstrate the drug loading and the presence of some interactions between the polymer matrix and loaded drugs. In vitro viability was studied on 4T1 mammary carcinoma mouse cells as a function of time and concentration of drug-loaded PMs. UA-PMs and free PMs alone were not effective in inhibiting the tumor cell growth whereas a viability of 40% was determined for cells treated with both PTX- and PTX/UA-loaded PMs. A synergic effect was noticed for PTX/UA-loaded PMs. Full article
(This article belongs to the Special Issue Drug-Loaded Polymer Colloidal Systems in Nanomedicine III)
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