In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide

This study reports on the release of a novel natriuretic peptide, CD-NP, from an in situ polymer precipitation delivery system. Following extensive screening of in-vitro release profiles, an in-vivo evaluation of the efficacy of the delivery system was carried out in Wistar rats. Gel injection was p...

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Main Authors: Venkatraman, Subbu S., Burnett Jr, John C., Chen, Horng H., Lim, Soo Ghim
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/96294
http://hdl.handle.net/10220/11906
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-962942023-07-14T15:53:49Z In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide Venkatraman, Subbu S. Burnett Jr, John C. Chen, Horng H. Lim, Soo Ghim School of Materials Science & Engineering This study reports on the release of a novel natriuretic peptide, CD-NP, from an in situ polymer precipitation delivery system. Following extensive screening of in-vitro release profiles, an in-vivo evaluation of the efficacy of the delivery system was carried out in Wistar rats. Gel injection was performed subcutaneously on the back of the rats. A secondary messenger, cyclic Guanosine 3′5′ Monophosphate (cGMP), was tested for verification of CD-NP bioactivity, in addition to direct measurements of CD-NP levels in plasma and urine using a radio-immuno assay. Plasma evaluation showed an elevated level of CD-NP over 3 weeks' duration. Unexpectedly, plasma cGMP level followed a decreasing trend over the same duration despite high CD-NP level. Loss of drug bioactivity was ruled out as a high level of CD-NP and cGMP excretion was observed in the treatment group as compared to baseline readings. This unexpected low-plasma cGMP levels and high-urinary cGMP excretion suggest that there might be other compensatory responses to regulation of the CDNP bioactivity as a result of the high drug dosing. The results stress the importance of assessing the overall bioactivity of released drug (in-vivo) concurrently in addition to measuring its concentrations, to determine the correct release profile. Published version 2013-07-22T02:08:55Z 2019-12-06T19:28:19Z 2013-07-22T02:08:55Z 2019-12-06T19:28:19Z 2013 2013 Journal Article Lim, S. G., Venkatraman, S. S., Burnett Jr, J. C., & Chen, H. H. (2013). In-Vivo Evaluation of an In Situ Polymer Precipitation Delivery System for a Novel Natriuretic Peptide. PLoS ONE, 8(2), e52484. 1932-6203 https://hdl.handle.net/10356/96294 http://hdl.handle.net/10220/11906 10.1371/journal.pone.0052484 23441143 171886 en PLoS One © 2013 The Authors. This paper was published in PLoS ONE and is made available as an electronic reprint (preprint) with permission of The Authors. The paper can be found at the following official DOI: [http://dx.doi.org/10.1371/journal.pone.0052484]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
description This study reports on the release of a novel natriuretic peptide, CD-NP, from an in situ polymer precipitation delivery system. Following extensive screening of in-vitro release profiles, an in-vivo evaluation of the efficacy of the delivery system was carried out in Wistar rats. Gel injection was performed subcutaneously on the back of the rats. A secondary messenger, cyclic Guanosine 3′5′ Monophosphate (cGMP), was tested for verification of CD-NP bioactivity, in addition to direct measurements of CD-NP levels in plasma and urine using a radio-immuno assay. Plasma evaluation showed an elevated level of CD-NP over 3 weeks' duration. Unexpectedly, plasma cGMP level followed a decreasing trend over the same duration despite high CD-NP level. Loss of drug bioactivity was ruled out as a high level of CD-NP and cGMP excretion was observed in the treatment group as compared to baseline readings. This unexpected low-plasma cGMP levels and high-urinary cGMP excretion suggest that there might be other compensatory responses to regulation of the CDNP bioactivity as a result of the high drug dosing. The results stress the importance of assessing the overall bioactivity of released drug (in-vivo) concurrently in addition to measuring its concentrations, to determine the correct release profile.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Venkatraman, Subbu S.
Burnett Jr, John C.
Chen, Horng H.
Lim, Soo Ghim
format Article
author Venkatraman, Subbu S.
Burnett Jr, John C.
Chen, Horng H.
Lim, Soo Ghim
spellingShingle Venkatraman, Subbu S.
Burnett Jr, John C.
Chen, Horng H.
Lim, Soo Ghim
In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
author_sort Venkatraman, Subbu S.
title In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
title_short In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
title_full In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
title_fullStr In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
title_full_unstemmed In-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
title_sort in-vivo evaluation of an in situ polymer precipitation delivery system for a novel natriuretic peptide
publishDate 2013
url https://hdl.handle.net/10356/96294
http://hdl.handle.net/10220/11906
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