Herein, chitosan has been functionalized with four nucleobases to investigate its mucoadhesive properties in the hydrogel form. These nucleobase-modified polymers were characterized by NMR, FT-IR, EDAX, TGA and evaluated for its ROS responsive degradation, cytocompatibility, mucoadhesion, hemocompatibility, anti-bacterial, anti-fungal and biofilm inhibitory properties. All the conjugated polymers have shown superior mucoadhesion along with the cyto- and hemo- compatibility as compared to chitosan. These functionalized polymers have shown excellent anti-bacterial activity against E. coli and S. aureus. In particular, the guanine-conjugated polymer (P4) showcased excellent mucoadhesive properties. This finding corroborated the in-silico prediction of the interaction of chitosan and conjugated chitosan polymers with the mucin. All modified chitosans possess potent anti-fungal activity for Candida albicans, Candida tropicalis and Candida glabrata along with the anti-biofilm properties for Candida tropicalis. P4 was found to reduce the multilayer polymicrobial biofilms consisting of bacterial and fungal species to a single layer. In addition, P4 as hydrogel scaffold has demonstrated excellent mucoadhesion and tissue adhesion. P4 hydrogel was found to release the anti-inflammatory drug diclofenac in ROS responsive manner. Hydrogel P4 displayed effectiveness in oral wound healing properties in-vivo in the case of an oral mucositis rat model.
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http://dx.doi.org/10.1016/j.carbpol.2025.123353 | DOI Listing |
Biotechnol Appl Biochem
March 2025
Department of Respiratory and Critical Care Medicine, The 2nd Medical Centre, Chinese PLA General Hospital, Beijing, PR China.
Employing an active targeting method with monoclonal antibodies for chemotherapeutics-loaded nanocarriers represents a promising option to enhance the specific drug delivery and alleviate the detrimental effects of chemotherapeutic agents. Targeted delivery to the human epidermal growth factor receptor-2 (HER2), which is overexpressed in HER2+ lung cancerous cells, can be accomplished by conjugating nanoparticles with a monoclonal antibody (anti-HER2). We developed trastuzumab (TZ)-conjugated chitosan iodoacetamide (CsIA)-coated liposomal nanoparticles carrying SN-38 (TZ-SN-CsIA LNPs) as a lung-targeted delivery.
View Article and Find Full Text PDFACS Appl Bio Mater
March 2025
Rubber Technology Centre, Indian Institute of Technology, Kharagpur 721302, India.
The favorable success rate in cancer treatment predominantly depends on precise diagnosis with target-specific drug delivery, which can regulate the patient survival outcome rate. Moreover, proper tracking of the system's pH is very much crucial as most of the therapeutic's action and release rate depend on it. Therefore, this work has been intended to fabricate a folic acid-derived carbon dot (FACD) decorated with chitosan (Cs) in order to form nanospheres (FACD-Cs-Ns) for anticancer doxorubicin hydrochloride (Dox.
View Article and Find Full Text PDFInt J Biol Macromol
March 2025
Department of Food Science and Engineering, Jinan University, Guangzhou 510632, China; Guangdong-Hong Kong Joint Innovation Platform of Baked Food Safety, Guangzhou 510632, China. Electronic address:
Carbonyl stress contributes to pathological disorders leading to the progression of a variety of chronic diseases. Exploration of food ingredients with carbonyl scavenging capacities became one of the most potential strategies for the prevention of these diseases. Polysaccharide-based hydrocolloids have wide application approaches in the food industry.
View Article and Find Full Text PDFAAPS PharmSciTech
March 2025
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, 11724, USA.
This study introduces advanced nanoparticle-based drug delivery systems (NDDS) designed for targeted colorectal cancer treatment. We developed and characterized three distinct formulations: Bevacizumab-loaded chitosan nanoparticles (BEV-CHI-NP), polymeric micelles (BEV-PM), and BEV-conjugated exosomes enriched with AS1411 and N1-methyladenosine (AP-BEV + M1A-EXO). Each formulation exhibited optimized physicochemical properties, with particle sizes between 150 and 250 nm and surface charges ranging from + 14.
View Article and Find Full Text PDFCarbohydr Polym
May 2025
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), Ahmedabad, Gujarat 382355, India. Electronic address:
Herein, chitosan has been functionalized with four nucleobases to investigate its mucoadhesive properties in the hydrogel form. These nucleobase-modified polymers were characterized by NMR, FT-IR, EDAX, TGA and evaluated for its ROS responsive degradation, cytocompatibility, mucoadhesion, hemocompatibility, anti-bacterial, anti-fungal and biofilm inhibitory properties. All the conjugated polymers have shown superior mucoadhesion along with the cyto- and hemo- compatibility as compared to chitosan.
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