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Synthesis and characterization of a novel pH-responsive drug-releasing nanocomposite hydrogel for skin cancer therapy and wound healing.
Gonsalves, Andrea; Tambe, Pranjali; Le, Duong; Thakore, Dheeraj; Wadajkar, Aniket S; Yang, Jian; Nguyen, Kytai T; Menon, Jyothi U.
Afiliação
  • Gonsalves A; Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, 7 Greenhouse Road, Kingston, RI 02881, USA. jmenon@uri.edu.
  • Tambe P; Department of Bioengineering, University of Texas at Arlington, Arlington, TX 76019, USA.
  • Le D; Department of Biomedical Engineering, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Thakore D; Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, 7 Greenhouse Road, Kingston, RI 02881, USA. jmenon@uri.edu.
  • Wadajkar AS; Department of Bioengineering, University of Texas at Arlington, Arlington, TX 76019, USA.
  • Yang J; Department of Biomedical Engineering, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
  • Nguyen KT; Department of Bioengineering, University of Texas at Arlington, Arlington, TX 76019, USA.
  • Menon JU; Department of Biomedical Engineering, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
J Mater Chem B ; 9(46): 9533-9546, 2021 12 01.
Article em En | MEDLINE | ID: mdl-34757371
ABSTRACT
Local skin cancer recurrence occurs in ∼12% of the patients post-surgery due to persistent growth of residual cancer cells. Wound infection is another significant complication following surgery. We report a novel in situ-forming nanocomposite hydrogel (NCH) containing PLGA-carboxymethyl chitosan nanoparticles (186 nm) for localized pH-responsive skin cancer therapy and wound healing. This injectable hydrogel, comprising of a citric acid-derived polymer backbone, gelled within 5 minutes, and demonstrated excellent swelling (283% of dry weight) and compressive strengths (∼5.34 MPa). Nanoparticle incorporation did not significantly affect hydrogel properties. The NCH effluents were cytocompatible with human dermal fibroblasts at 500 µg ml-1 concentration and demonstrated pH-dependent drug release and promising therapeutic efficacy against A431 and G361 skin cancer cells in vitro. Significant zones of inhibition were observed in S. aureus and E. coli cultures on NCH treatment, confirming its antibacterial properties. Our studies show that the pH-responsive NCH can be potentially used for adjuvant skin cancer treatment and wound healing.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Neoplasias Cutâneas / Hidrogéis / Quitosana / Nanocompostos Limite: Humans Idioma: En Revista: J Mater Chem B Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Neoplasias Cutâneas / Hidrogéis / Quitosana / Nanocompostos Limite: Humans Idioma: En Revista: J Mater Chem B Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos