Ionic cross‐linking of water‐soluble polyurethane improves protein encapsulation and release. Issue 4 (30th March 2015)
- Record Type:
- Journal Article
- Title:
- Ionic cross‐linking of water‐soluble polyurethane improves protein encapsulation and release. Issue 4 (30th March 2015)
- Main Title:
- Ionic cross‐linking of water‐soluble polyurethane improves protein encapsulation and release
- Authors:
- Mattu, Clara
Wang, Tianran
Siri, Armida
Sartori, Susanna
Ciardelli, Gianluca - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Polymer nanoparticles (NPs) are promising systems for the delivery of protein drugs, as they enhance circulation half‐life, reduce degradation, and increase selectivity of the encapsulated agent. Among the different methods for the preparation of protein‐loaded NPs, ionotropic gelation—which exploits cross‐linking between charged groups in the polymer and counterions in the protein solution—has been extensively investigated for chitosan NPs. The present study aims at exploring the possibility to apply the method to prepare BSA‐loaded polyurethane NPs. A poly(ε‐caprolactone)/poly(ethyleneglicol)‐based polyurethane bearing <italic>tert</italic>‐butyloxycarbonyl‐protected amino groups was synthesized by a two‐step synthesis procedure. Amino functionalities were exposed under acidic conditions, as confirmed by ninhydrin assay, and then exploited to obtain ionic cross‐linking with sodium tripolyphosphate counterions. The effect of polymer and sodium tripolyphosphate concentration on particles size and BSA encapsulation has been investigated, showing that the PUR concentration plays a major role. Small particles, at 300 nm, with high BSA loading (90%) have been obtained. Sustained BSA release and low burst effect (20%) have been observed, indicating good interaction between the protein and the polymer matrix. The study highlights the possibility of introducing alternative polymers to improve<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Polymer nanoparticles (NPs) are promising systems for the delivery of protein drugs, as they enhance circulation half‐life, reduce degradation, and increase selectivity of the encapsulated agent. Among the different methods for the preparation of protein‐loaded NPs, ionotropic gelation—which exploits cross‐linking between charged groups in the polymer and counterions in the protein solution—has been extensively investigated for chitosan NPs. The present study aims at exploring the possibility to apply the method to prepare BSA‐loaded polyurethane NPs. A poly(ε‐caprolactone)/poly(ethyleneglicol)‐based polyurethane bearing <italic>tert</italic>‐butyloxycarbonyl‐protected amino groups was synthesized by a two‐step synthesis procedure. Amino functionalities were exposed under acidic conditions, as confirmed by ninhydrin assay, and then exploited to obtain ionic cross‐linking with sodium tripolyphosphate counterions. The effect of polymer and sodium tripolyphosphate concentration on particles size and BSA encapsulation has been investigated, showing that the PUR concentration plays a major role. Small particles, at 300 nm, with high BSA loading (90%) have been obtained. Sustained BSA release and low burst effect (20%) have been observed, indicating good interaction between the protein and the polymer matrix. The study highlights the possibility of introducing alternative polymers to improve loading and release of proteins from NPs obtained through the ionotropic gelation method.</p> </abstract> … (more)
- Is Part Of:
- Engineering in life sciences. Volume 15:Issue 4(2015)
- Journal:
- Engineering in life sciences
- Issue:
- Volume 15:Issue 4(2015)
- Issue Display:
- Volume 15, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 15
- Issue:
- 4
- Issue Sort Value:
- 2015-0015-0004-0000
- Page Start:
- 448
- Page End:
- 455
- Publication Date:
- 2015-03-30
- Subjects:
- Bioengineering -- Periodicals
660.605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1618-2863 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/elsc.201400188 ↗
- Languages:
- English
- ISSNs:
- 1618-0240
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3764.680000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3562.xml