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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/13707
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dc.contributor.authorChitkara, Deepak-
dc.contributor.authorMittal, Anupama-
dc.date.accessioned2024-01-06T06:25:52Z-
dc.date.available2024-01-06T06:25:52Z-
dc.date.issued2024-01-
dc.identifier.urihttps://jpet.aspetjournals.org/content/388/1/37.abstract-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13707-
dc.description.abstractProtein and peptide therapeutics score better than small-molecule therapeutics owing to their higher potency, greater specificity, and fewer immunological responses. Furthermore, they also have an advantage over gene therapy in terms of being safer since these involve a downstream regulation mechanism and do not alter the genetic machinery. Due to their unique advantages, there are currently more than 80 peptide drugs in the global market, with insulin and its analogs responsible for 50% of the peptide drug revenue. There are also 150 peptide drugs in the clinical pipeline and another 400–600 undergoing preclinical studies. Proteins and peptides are investigated for several therapeutic purposes, including cytokines, antibodies, enzymes, tumor antigens, and proapoptotic proteins/peptides. Although the market for protein-based therapeutics shows potential and is rapidly expandingen_US
dc.language.isoenen_US
dc.publisherASPETen_US
dc.subjectPharmacyen_US
dc.subjectNanotechnology-Based Deliveryen_US
dc.subjectProteinen_US
dc.titleSpecial Section on Nanotechnology-Based Delivery Strategies for Protein and Peptide Therapeutics—Editorialen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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