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Application of QbD Principles in Nanocarrier-Based Drug Delivery Systems

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dc.contributor.author Singhvi, Gautam
dc.date.accessioned 2024-01-10T09:21:46Z
dc.date.available 2024-01-10T09:21:46Z
dc.date.issued 2019
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/B9780128157992000149
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13780
dc.description.abstract Development of nanomedicines has become an attractive strategy in the delivery of therapeutics to overcome the problems associated with conventional therapy especially for cancer, skin infections, tuberculosis, and other long-term disorders. Preparation of nanocarriers includes multiple constituents and multiple steps which need to be understood in-depth. It is expected that the application of quality by design (QbD) approach can overcome the existing issues related to nanoformulation development and can provide wider acceptability for regulatory agencies to form constructive guidelines for their approval. The objective of QbD in nanocarrier drug delivery is to derive meaningful product specifications based on safety, efficacy, and clinical performance. It helps in investigation of variable factors with respect to materials and process involved and ultimately enhances the process capability with minimum product variability. This book chapter has compiled various QbD components which can be easily implemented for preparation and optimization of robust nanoformulations. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Pharmacy en_US
dc.subject Nanomedicines en_US
dc.subject Nanocarriers en_US
dc.subject Quality-by design en_US
dc.subject Critical material attributes en_US
dc.subject Critical quality attributes en_US
dc.subject Process variables en_US
dc.title Application of QbD Principles in Nanocarrier-Based Drug Delivery Systems en_US
dc.type Book chapter en_US


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