Er. Akshit Kohli
ABESIT Engineering College
Crossings Republik, Ghaziabad, Uttar Pradesh 201009
Abstract
Biodegradable polymers have emerged as an innovative platform for controlled drug release systems, offering significant advantages in terms of safety, efficacy, and patient compliance. This study investigates the synthesis, characterization, and application of novel biodegradable polymer matrices designed for the sustained release of therapeutic agents. By tailoring polymer composition and degradation profiles, the controlled release system ensures a consistent drug concentration over extended periods, thereby minimizing side effects and improving treatment outcomes. A comprehensive literature review up to 2017 was conducted to identify existing methodologies, limitations, and promising advancements. Statistical analyses were performed on in vitro release data, validating the consistency and reliability of the developed formulations. The results indicate that polymer modifications, such as copolymer blending and crosslinking density adjustments, significantly influence the degradation kinetics and drug release profiles. Furthermore, the optimized biodegradable systems exhibit a biphasic release pattern, characterized by an initial burst followed by a sustained release phase. This manuscript discusses the experimental approach, the statistical methods used for data analysis, and the implications of the findings. In conclusion, the developed biodegradable polymer systems not only promise improved therapeutic management but also open avenues for customizable drug delivery applications. Future research should focus on in vivo evaluations and scaling up the technology for clinical applications.
Keywords
Biodegradable polymers; controlled drug release; polymer degradation; sustained delivery; formulation optimization
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