Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems

Different synthetic strategies were tested for the incorporation of galactose molecules on thermoresponsive nanogels owing to their affinity for receptors expressed in cancer cells. Three families of galactose-functionalized poly(<i>N</i>-vinylcaprolactam) nanogels were prepared with the...

Full description

Bibliographic Details
Main Authors: Mirian A. González-Ayón, Angel Licea-Claverie, J. Adriana Sañudo-Barajas
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/12/9/2150
id doaj-7c4e4fd9c044437ea8e1c6cfea3c5bc5
record_format Article
spelling doaj-7c4e4fd9c044437ea8e1c6cfea3c5bc52020-11-25T03:54:58ZengMDPI AGPolymers2073-43602020-09-01122150215010.3390/polym12092150Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery SystemsMirian A. González-Ayón0Angel Licea-Claverie1J. Adriana Sañudo-Barajas2Centro de Graduados e Investigación en Química, Tecnológico Nacional de México/Instituto Tecnológico de Tijuana, Apartado Postal 1166, Tijuana 22454, MexicoCentro de Graduados e Investigación en Química, Tecnológico Nacional de México/Instituto Tecnológico de Tijuana, Apartado Postal 1166, Tijuana 22454, MexicoCentro de Investigación en Alimentación y Desarrollo, A. C. Carretera a El dorado Km 5.5, Culiacán 80110, MexicoDifferent synthetic strategies were tested for the incorporation of galactose molecules on thermoresponsive nanogels owing to their affinity for receptors expressed in cancer cells. Three families of galactose-functionalized poly(<i>N</i>-vinylcaprolactam) nanogels were prepared with the aim to control the introduction of galactose-moieties into the core, the core-shell interface and the shell. First and second of the above mentioned, were prepared via surfactant free emulsion polymerization (SFEP) by a free-radical mechanism and the third one, via SFEP/reversible addition-fragmentation chain transfer (RAFT) polymerization. Synthetic recipes for the SFEP/free radical method included besides <i>N</i>-vinylcaprolactam (NVCL), a shell forming poly(ethylene glycol) methyl ether methacrylate (PEGMA), while the galactose (GAL) moiety was introduced via 6-O-acryloyl-1,2,:3,4-bis-O-(1-methyl-ethylidene)-α-<sub>D</sub>-galactopiranose (6-ABG, protected GAL-monomer): nanogels I, or 2-lactobionamidoethyl methacrylate (LAMA, GAL-monomer): nanogels II. For the SFEP/RAFT methodology poly(2-lactobionamidoethyl methacrylate) as GAL macro-chain transfer agent (PLAMA macro-CTA) was first prepared and on a following stage, the macro-CTA was copolymerized with PEGMA and NVCL, nanogels III. The crosslinker ethylene glycol dimethacrylate (EGDMA) was added in both methodologies for the polymer network construction. Nanogel’s sizes obtained resulted between 90 and 370 nm. With higher content of PLAMA macro-CTA or GAL monomer in nanogels, a higher the phase-transition temperature (T<sub>VPT</sub>) was observed with values ranging from 28 to 46 °C. The ρ-parameter, calculated by the ratio of gyration and hydrodynamic radii from static (SLS) and dynamic (DLS) light scattering measurements, and transmission electron microscopy (TEM) micrographs suggest that core-shell nanogels of flexible chains were obtained; in either spherical (nanogels II and III) or hyperbranched (nanogels I) form.https://www.mdpi.com/2073-4360/12/9/2150thermoresponsive nanogelsRAFTSFEP<i>N</i>-vinylcaprolactamgalactose-functionalized nanogels
collection DOAJ
language English
format Article
sources DOAJ
author Mirian A. González-Ayón
Angel Licea-Claverie
J. Adriana Sañudo-Barajas
spellingShingle Mirian A. González-Ayón
Angel Licea-Claverie
J. Adriana Sañudo-Barajas
Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems
Polymers
thermoresponsive nanogels
RAFT
SFEP
<i>N</i>-vinylcaprolactam
galactose-functionalized nanogels
author_facet Mirian A. González-Ayón
Angel Licea-Claverie
J. Adriana Sañudo-Barajas
author_sort Mirian A. González-Ayón
title Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems
title_short Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems
title_full Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems
title_fullStr Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems
title_full_unstemmed Different Strategies for the Preparation of Galactose-Functionalized Thermo-Responsive Nanogels with Potential as Smart Drug Delivery Systems
title_sort different strategies for the preparation of galactose-functionalized thermo-responsive nanogels with potential as smart drug delivery systems
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2020-09-01
description Different synthetic strategies were tested for the incorporation of galactose molecules on thermoresponsive nanogels owing to their affinity for receptors expressed in cancer cells. Three families of galactose-functionalized poly(<i>N</i>-vinylcaprolactam) nanogels were prepared with the aim to control the introduction of galactose-moieties into the core, the core-shell interface and the shell. First and second of the above mentioned, were prepared via surfactant free emulsion polymerization (SFEP) by a free-radical mechanism and the third one, via SFEP/reversible addition-fragmentation chain transfer (RAFT) polymerization. Synthetic recipes for the SFEP/free radical method included besides <i>N</i>-vinylcaprolactam (NVCL), a shell forming poly(ethylene glycol) methyl ether methacrylate (PEGMA), while the galactose (GAL) moiety was introduced via 6-O-acryloyl-1,2,:3,4-bis-O-(1-methyl-ethylidene)-α-<sub>D</sub>-galactopiranose (6-ABG, protected GAL-monomer): nanogels I, or 2-lactobionamidoethyl methacrylate (LAMA, GAL-monomer): nanogels II. For the SFEP/RAFT methodology poly(2-lactobionamidoethyl methacrylate) as GAL macro-chain transfer agent (PLAMA macro-CTA) was first prepared and on a following stage, the macro-CTA was copolymerized with PEGMA and NVCL, nanogels III. The crosslinker ethylene glycol dimethacrylate (EGDMA) was added in both methodologies for the polymer network construction. Nanogel’s sizes obtained resulted between 90 and 370 nm. With higher content of PLAMA macro-CTA or GAL monomer in nanogels, a higher the phase-transition temperature (T<sub>VPT</sub>) was observed with values ranging from 28 to 46 °C. The ρ-parameter, calculated by the ratio of gyration and hydrodynamic radii from static (SLS) and dynamic (DLS) light scattering measurements, and transmission electron microscopy (TEM) micrographs suggest that core-shell nanogels of flexible chains were obtained; in either spherical (nanogels II and III) or hyperbranched (nanogels I) form.
topic thermoresponsive nanogels
RAFT
SFEP
<i>N</i>-vinylcaprolactam
galactose-functionalized nanogels
url https://www.mdpi.com/2073-4360/12/9/2150
work_keys_str_mv AT mirianagonzalezayon differentstrategiesforthepreparationofgalactosefunctionalizedthermoresponsivenanogelswithpotentialassmartdrugdeliverysystems
AT angelliceaclaverie differentstrategiesforthepreparationofgalactosefunctionalizedthermoresponsivenanogelswithpotentialassmartdrugdeliverysystems
AT jadrianasanudobarajas differentstrategiesforthepreparationofgalactosefunctionalizedthermoresponsivenanogelswithpotentialassmartdrugdeliverysystems
_version_ 1724471574901293056