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Orally Administered, Biodegradable and Biocompatible Hydroxypropyl-β-Cyclodextrin Grafted Poly(methacrylic acid) Hydrogel for pH Sensitive Sustained Anticancer Drug Delivery. | LitMetric

AI Article Synopsis

  • A pH-sensitive hydrogel made from hydroxypropyl-β-cyclodextrin and methacrylic acid was created for targeted delivery of cytarabine in the colon.
  • The hydrogels showed a loading capacity for cytarabine between 37.17% and 79.3% and released the drug in a controlled manner over 24 hours, especially at intestinal pH.
  • Toxicity tests confirmed that the hydrogels were safe for use and they had a longer plasma half-life compared to conventional oral cytarabine, making them promising for colon cancer treatment.

Article Abstract

In the current study, a pH sensitive intelligent hydroxypropyl-β-cyclodextrin-based polymeric network (HP-β-CD-g-MAA) was developed through a solution polymerization technique for site specific delivery of cytarabine in the colonic region. Prepared hydrogel formulations were characterized through cytarabine loading (%), ingredient's compatibility, structural evaluation, thermal integrity, swelling pattern, release behavior and toxicological profiling in rabbits. Moreover, the pharmacokinetic profile of cytarabine was also determined in rabbits. New polymer formation was evident from FTIR findings. The percentage loaded into the hydrogels was in the range of 37.17-79.3%. Optimum swelling ratio of 44.56 was obtained at pH 7.4. Cytarabine release was persistent and in a controlled manner up to 24 h. In vitro degradation of hydrogels was more pronounced at intestinal pH as compared to acidic pH. Toxicity studies proved absence of any ocular, skin and oral toxicity, thus proving biocompatibility of the fabricated network. Hydrogels exhibited longer plasma half-life (8.75 h) and AUC (45.35 μg.h/mL) with respect to oral cytarabine solution. Thus, the developed hydrogel networks proved to be excellent and biocompatible cargo for prolonged and site-specific delivery of cytarabine in the management of colon cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953841PMC
http://dx.doi.org/10.3390/gels8030190DOI Listing

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