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Original Abstract of the Article :
The influence of buffer composition on the release of cefuroxime axetil from stearic acid microspheres has been investigated, with particular emphasis on establishing the relationship between buffer composition and release at a single pH value. Studies of drug dissolution and release from spheres in...See full text at original site
Dr.Camel's Paper Summary Blogラクダ博士について
ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
難解な医学論文を、専門知識のない方にも理解しやすいように、噛み砕いて説明することを目指しています。
* ラクダ博士による解説は、あくまで論文の要点をまとめたものであり、原論文の完全な代替となるものではありません。詳細な内容については、必ず原論文をご参照ください。
* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。
引用元:
https://doi.org/10.1016/s0378-5173(99)00391-9
データ提供:米国国立医学図書館(NLM)
Unraveling the Secrets of Cefuroxime Axetil Release
The field of [pharmaceutical formulation] seeks to optimize drug delivery for enhanced effectiveness and patient outcomes. This study, like a chemist meticulously exploring the properties of different substances, examines the release of cefuroxime axetil from taste-masked stearic acid microspheres, a formulation designed for efficient drug delivery. The researchers, like skilled engineers constructing a complex system, investigate the impact of buffer composition on drug release, seeking to understand the factors that influence drug delivery. Their findings reveal a complex relationship between buffer composition and release rate, providing valuable insights for optimizing drug formulation and ensuring effective drug delivery. This study offers a detailed understanding of the factors influencing drug release from microspheres, providing valuable information for pharmaceutical development and clinical practice.
The Influence of Buffer Composition on Drug Release
The study's findings indicate that [marked differences in release profile from the spheres, with an approximate rank order of SMPB > CPB approximately BAB > PBM] were observed. The researchers also discovered that [increases in the sodium content from approximately 0.11 to 0.2 M were found to decrease the release rate for the SMPB, while increases from 0.007 to 1.0 M sodium in PBM resulted in a maximum release being seen for the systems containing 0.05 M sodium]. These observations highlight the complex interplay of buffer composition and drug release, emphasizing the need for careful consideration of these factors during formulation development. It's like navigating a desert landscape, understanding the impact of different terrain on travel and choosing the optimal route for a successful journey.
Optimizing Drug Delivery for Enhanced Patient Outcomes
This study's insights are valuable for pharmaceutical companies and researchers developing new drug formulations. By understanding the impact of buffer composition on drug release, they can optimize formulations to ensure efficient drug delivery and maximize patient outcomes. It's like discovering a hidden oasis with a plentiful water source, ensuring that the traveler reaches their destination refreshed and rejuvenated.
Dr.Camel's Conclusion
This study takes us on a fascinating journey into the complexities of drug release, highlighting the importance of buffer composition in optimizing drug delivery. By understanding the intricate relationship between buffer composition and release rate, pharmaceutical scientists can develop more effective and patient-friendly formulations. As Dr. Camel, I believe that continuous exploration and refinement of drug delivery methods will lead to a brighter future for patients, ensuring that their journeys to health and well-being are as smooth and efficient as possible.
Date :
- Date Completed 2000-04-03
- Date Revised 2019-09-10
Further Info :
Related Literature
English
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