Kappa-carrageenan and sodium alginate-based pH-responsive hydrogels for controlled release of methotrexate

Author:

Anees Ur Rehman Qureshi Muhammad1,Arshad Nasima1ORCID,Rasool Atta2ORCID,Janjua Naveed Kausar3,Butt Muhammad Shoaib4,Naqeeb Ur Rehman Qureshi Muhammad5,Ismail Hammad6

Affiliation:

1. Department of Chemistry, Allama Iqbal Open University , Islamabad, Pakistan

2. School of Chemistry, University of the Punjab , Lahore, Pakistan

3. Department of Chemistry, Quaid-i-Azam University , Islamabad, Pakistan

4. School of Chemical and Materials Engineering (SCME), National University of Science and Technology , Islamabad 44000, Pakistan

5. Faculty of Sciences, Department of Zoology and Biology, Pir Mehr Ali Shah ARID Agriculture University , Rawalpindi, Pakistan

6. Department of Biochemistry and Biotechnology, University of Gujrat , Gujrat, 50700 , Pakistan

Abstract

Despite remarkable progress in medical sciences, modern man is still fighting the battle against cancer. In 2022, only in the USA, 640 000 deaths and 2 370 000 patients were reported because of cancer. Chemotherapy is the most widely used for cancer treatments. However, chemotherapeutics have severe physicochemical side effects. Therefore, we have prepared poly(amididoamine) dendrimeric carrageenan (CG), sodium alginate (SA) and poly(vinyl alcohol) (PVA) hydrogels by using solution casting methodology. The constituents of hydrogels were cross-linked by mutable quantity of 3-aminopropyl(diethoxy)methyl silane (APDMS). Hydrogels were characterized by Fourier transform infrared spectroscopy, thermal gravimetric analysis, scanning electron microscope and atomic force microscopy. Hydrogels exhibited higher swelling volumes in 5–7 pH range. In vitro biodegradation in ribonuclease-A solution and cytocompatibility analysis against DF-1 fibroblasts established their biodegradable and non-toxic nature, which enables them as a suitable carrier for chemotherapeutic compounds. Hence, methotrexate (MTX) as a model drug was loaded on CAP-8 hydrogel and its release was detected by the UV–visible spectrophotometer in phosphate-buffered saline (PBS) solution. In 13.5 h, 81.25% and 77.23% of MTX were released at pH 7.4 (blood pH) and 5.3 (tumour pH) in PBS, respectively. MTX was released by super case II mechanism and best fitted to zero-order and Korsmeyer–Peppas model. The synthesized APDMS cross-linked CG/SA/PVA dendrimeric hydrogels could be an efficient model platform for the effective delivery of MTX in cancer treatments.

Publisher

The Royal Society

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