Newer Insulin Preparations and Insulin Analogs
- PMID: 39734941
- PMCID: PMC11676328
- DOI: 10.7759/cureus.74593
Newer Insulin Preparations and Insulin Analogs
Abstract
Diabetes mellitus represents a significant and growing global health challenge, with its prevalence steadily increasing. Insulin therapy remains a cornerstone of diabetes management. Since its discovery in 1921, insulin has undergone substantial advancements, evolving from crude animal extracts to highly refined recombinant formulations and biosimilars. This review explores the progression of insulin therapies, emphasizing the evolution from conventional insulins to modern analogs designed to mimic endogenous insulin more effectively. The limitations of early insulin formulations, such as unpredictable absorption, rigid dosing regimens, and an increased risk of hypoglycemia, highlighted the need for improved therapies. Modern insulin analogs, including fast-acting (e.g., insulin lispro), long-acting (e.g., insulin glargine and insulin degludec), and ultra-long-acting (e.g., insulin icodec) options, address these challenges by providing stable and consistent pharmacokinetics, along with enhanced glycemic control. Furthermore, biosimilar insulins, produced via recombinant DNA technology, have increased accessibility while maintaining therapeutic efficacy and safety. Recent innovations, such as ultra-long-acting insulins and combination therapies like insulin icodec with semaglutide, offer the potential to reduce injection frequency and enable personalized diabetes care. These advancements contribute to improved patient compliance, reduced glycemic variability, and an enhanced quality of life. This review highlights the critical role of ongoing research and innovation in insulin therapy to meet the evolving needs of diabetes management.
Keywords: diabetes mellitus type i; frederick banting; long-acting insulin; porcine; reference insulin glargine.
Copyright © 2024, Tiwari et al.
Conflict of interest statement
Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Figures
References
-
- Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: results from the International Diabetes Federation Diabetes Atlas, 9th edition. Saeedi P, Petersohn I, Salpea P, et al. Diabetes Res Clin Pract. 2019;157:107843. - PubMed
-
- Insulin lispro: a fast-acting insulin analog. Noble SL, Johnston E, Walton B. https://www.aafp.org/pubs/afp/issues/1998/0115/p279.html. Am Fam Physician. 1998;57:279–286. - PubMed
-
- The History of a Wonderful Thing We Call Insulin. [ Mar; 2022 ];ADA ADA. https://diabetes.org/blog/history-wonderful-thing-we-call-insulin Diabetes.org. 2022 1:1.
Publication types
LinkOut - more resources
Full Text Sources