Development of polymeric IPN hydrogels by free radical polymerization technique for extended release of letrozole: Characterization and toxicity evaluation

Author:

Yousaf Hammad12,Khalid Ikrima1,Barkat Kashif3,Mehmood Yasir14,Badshah Syed Faisal3,Anjum Irfan5,Nafidi Hiba-Allah6,Bin Jardan Yousef A.7,Bourhia Mohammed8

Affiliation:

1. Department of Pharmaceutics, Government College University Faisalabad , Faisalabad , Pakistan

2. Rashid Latif College of Pharmacy, Rashid Latif Khan University , Lahore , Pakistan

3. Faculty of Pharmacy, The University of Lahore , Lahore , Pakistan

4. Riphah Institute of Pharmaceutical Sciences, Riphah International University , Faisalabad , Pakistan

5. Department of Basic Medical Sciences, Shifa College of Pharmaceutical Sciences, Shifa Tameer-e-Millat University Islamabad , Islamabad , Pakistan

6. Department of Food Science, Faculty of Agricultural and Food Sciences, Laval University , 2325 Quebec City , QC G1V 0A6 , Canada

7. Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 11451 , Riyadh , Saudi Arabia

8. Department of Chemistry and Biochemistry, Faculty of Medicine and Pharmacy, Ibn Zohr University , Laayoune 70000 , Morocco

Abstract

Abstract This research study’s objective was to formulate interpenetrating pH-sensitive polymeric networks interpenetrating networks (IPNs) based on hydroxypropylmethylcellulose (HPMC)/Primojel for use in the treatment of various malignant conditions. For controlled release, letrozole (LTZ) was selected as a model drug in HPMC and Primojel-based IPN hydrogels. HPMC and Primojel based IPN hydrogels were fabricated through the free radical polymerization method by utilizing HPMC and Primojel as polymers, methacrylic acid as monomer, ammonium persulfate as initiator, and methylenebisacrylamide as cross-linker. For structural characterization, various techniques such as Fourier transform infrared spectroscopy, Scanning electron microscopy (SEM), DSC, TGA, and Powder x-ray diffraction (PXRD) were applied to IPN samples. In vitro and swelling studies were also employed to observe the response of these polymeric networks against 1.2 and 7.4 pH. TGA and DSC of an optimized loaded formulation possess better thermal stability as compared to individual drug. PXRD depicted minor crystallinity and a significant amorphous nature. SEM images show that polymeric networks possess an uneven and porous surface. Significant swelling and enhanced in-vitro outcomes at a high pH of 7.4 confirmed the IPN pH responsive properties. Toxicological studies performed on rabbits revealed no harm in the results. Thus, IPN based on HPMC/Primojel was successfully synthesized and can be used for LTZ’s controlled release.

Publisher

Walter de Gruyter GmbH

Subject

Polymers and Plastics,Physical and Theoretical Chemistry,General Chemical Engineering

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