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A facile approach for thermal and reduction dual-responsive prodrug nanogels for intracellular doxorubicin delivery.
J Mater Chem B. 2016 Dec 21; 4(47):7572-7583.JM

Abstract

In this study, thermal and redox dual sensitive nanogels based on N-vinylcaprolactam (VCL) and N-succinimidyl methacrylate (Suma) crosslinked with diallyl disulfide were synthesized via a facile and straightforward method. The reactive succinimide groups were mainly located in the nanogel shell which increases considerably their accessibility for conjugation reactions. Doxorubicin (DOX) was successfully loaded into the nanogel through two different routes. Approximately 91.3% of DOX molecules were covalently bound to the nanogel network via coupling with succinimide groups under mild conditions to obtain prodrug nanogels, while 8.7% of DOX molecules were captured into the nanogels via electrostatic interactions with the -COOH group from the hydrolyzed ester groups of the nanogels. The DOX-loaded nanogels demonstrated volume phase transition temperature (VPTT) near human physiological temperature. The nanogels shrink near body temperature, which could help lock the drug molecules stably in blood circulation. The conjugation of DOX molecules in nanogels avoided premature unspecific drug release under physiological conditions. The small amount of physically loaded DOX (due to electrostatic interactions) could be partially released as free DOX due to the increasing acidic conditions in the endosome/lysosome pathway. The chemically conjugated DOX was released in the form of a prodrug polymer triggered by the high concentration of glutathione in the cytosol that induced nanogel degradation. The present drug delivery system exhibits a sustainable delivery profile in the intracellular release study and high antitumor activity. We are convinced that the thermal and reduction dual-responsive prodrug nanogels have tremendous potential in controlled drug release.

Authors+Show Affiliations

Functional and Interactive Polymers, Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, Aachen, Germany. pich@dwi.rwth-aachen.de.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

32263814

Citation

Peng, Huan, et al. "A Facile Approach for Thermal and Reduction Dual-responsive Prodrug Nanogels for Intracellular Doxorubicin Delivery." Journal of Materials Chemistry. B, vol. 4, no. 47, 2016, pp. 7572-7583.
Peng H, Huang X, Oppermann A, et al. A facile approach for thermal and reduction dual-responsive prodrug nanogels for intracellular doxorubicin delivery. J Mater Chem B. 2016;4(47):7572-7583.
Peng, H., Huang, X., Oppermann, A., Melle, A., Weger, L., Karperien, M., Wöll, D., & Pich, A. (2016). A facile approach for thermal and reduction dual-responsive prodrug nanogels for intracellular doxorubicin delivery. Journal of Materials Chemistry. B, 4(47), 7572-7583. https://doi.org/10.1039/c6tb01285j
Peng H, et al. A Facile Approach for Thermal and Reduction Dual-responsive Prodrug Nanogels for Intracellular Doxorubicin Delivery. J Mater Chem B. 2016 Dec 21;4(47):7572-7583. PubMed PMID: 32263814.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A facile approach for thermal and reduction dual-responsive prodrug nanogels for intracellular doxorubicin delivery. AU - Peng,Huan, AU - Huang,Xiaobin, AU - Oppermann,Alex, AU - Melle,Andrea, AU - Weger,Lindsey, AU - Karperien,Marcel, AU - Wöll,Dominik, AU - Pich,Andrij, Y1 - 2016/11/14/ PY - 2020/4/9/entrez SP - 7572 EP - 7583 JF - Journal of materials chemistry. B JO - J Mater Chem B VL - 4 IS - 47 N2 - In this study, thermal and redox dual sensitive nanogels based on N-vinylcaprolactam (VCL) and N-succinimidyl methacrylate (Suma) crosslinked with diallyl disulfide were synthesized via a facile and straightforward method. The reactive succinimide groups were mainly located in the nanogel shell which increases considerably their accessibility for conjugation reactions. Doxorubicin (DOX) was successfully loaded into the nanogel through two different routes. Approximately 91.3% of DOX molecules were covalently bound to the nanogel network via coupling with succinimide groups under mild conditions to obtain prodrug nanogels, while 8.7% of DOX molecules were captured into the nanogels via electrostatic interactions with the -COOH group from the hydrolyzed ester groups of the nanogels. The DOX-loaded nanogels demonstrated volume phase transition temperature (VPTT) near human physiological temperature. The nanogels shrink near body temperature, which could help lock the drug molecules stably in blood circulation. The conjugation of DOX molecules in nanogels avoided premature unspecific drug release under physiological conditions. The small amount of physically loaded DOX (due to electrostatic interactions) could be partially released as free DOX due to the increasing acidic conditions in the endosome/lysosome pathway. The chemically conjugated DOX was released in the form of a prodrug polymer triggered by the high concentration of glutathione in the cytosol that induced nanogel degradation. The present drug delivery system exhibits a sustainable delivery profile in the intracellular release study and high antitumor activity. We are convinced that the thermal and reduction dual-responsive prodrug nanogels have tremendous potential in controlled drug release. SN - 2050-7518 UR - https://www.unboundmedicine.com/medline/citation/32263814/A_facile_approach_for_thermal_and_reduction_dual_responsive_prodrug_nanogels_for_intracellular_doxorubicin_delivery_ DB - PRIME DP - Unbound Medicine ER -
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