Commercial challenges of protein drug delivery
- 1 January 2005
- journal article
- review article
- Published by Informa Healthcare in Expert Opinion on Drug Delivery
- Vol. 2 (1) , 29-42
- https://doi.org/10.1517/17425247.2.1.29
Abstract
The discovery of insulin in 1922 marked the beginning of research and development to improve the means of delivering protein therapeutics to patients. From that period forward, investigators have contemplated every possible route of delivery. Their research efforts have followed two basic pathways: one path has focused on non-invasive means of delivering proteins to the body; and the second path has been primarily aimed at increasing the biological half-life of the therapeutic molecules. Thus far, the commercial successes of protein delivery by the nasal, oral and pulmonary routes have been more opportunistic rather than the application of platform technologies applicable to every protein or peptide. In several limited cases, sustained delivery of p-eptides and proteins has employed the use of polymeric carriers. More successes have been achieved by chemical modification using amino acid sub-stitutions, protein pegylation or glycosylation to improve the pharmacodynamic properties of certain macromolecules...Keywords
This publication has 43 references indexed in Scilit:
- Alternative routes of insulin deliveryDiabetic Medicine, 2003
- Comparison of the Subcutaneous Absorption of Insulin Glargine (Lantus®) and NPH Insulin in Patients with Type 2 DiabetesHormone and Metabolic Research, 2003
- The Business of Insulin: A Relationship Between Innovation and EconomicsClinical Diabetes, 2003
- Peptide and protein PEGylation: a review of problems and solutionsPublished by Elsevier ,2001
- Infliximab for the Treatment of Fistulas in Patients with Crohn's DiseaseNew England Journal of Medicine, 1999
- Inhaled insulin1Abbreviations: DM, diabetes mellitus; AIDs, acquired immune deficiency syndrome; SC, subcutaneous; DCCT, Diabetes Control and Complications Trial; IDDM, insulin-dependent diabetes mellitus; NIDDM, non-insulin-dependent diabetes mellitus; i.v., intravenous; DDPC, di-decanoyl-alpha-phosphatidylcholine; AUC, area under the curve; INH, inhaled; Cmax, maximum serum concentration; Cmin, minimum serum concentration; Tmax, time of maximum serum concentration; NS, not significant; HbA1c, hemoglobin A1c; OA, oral agent; SD, standard deviation; MDI, metered dose inhaler; DPI, dry powder inhaler; MMAD, mass median aerodynamic diameter; CMC, critical micelle concentration; SR, sustained release; PLGA, poly lactic acid-co-glycolic acid; GI, gastrointestinal, GSD, geometric standard deviation; TLC, total lung capacity; VC, vital capacity; SMK, smokers; MW, molecular weight; MP, melting point.1Advanced Drug Delivery Reviews, 1999
- Renal Concentrating Capacity Test by Desmopressin in Children: Intranasal or Intravenous Route?American Journal of Nephrology, 1993
- The evolution and future of haemophilia therapyTransfusion Medicine, 1991
- Plasma Kinetics of DDAVP in ManActa Pharmacologica et Toxicologica, 1986
- The Origins of Hypodermic MedicationScientific American, 1971