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Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum
The administration of biological compounds that optimize health benefits is an ever-evolving therapeutic goal. Pharmaceutical and other adjunctive biological compounds have been administered via many different routes in order to produce a systemic pharmacological effect. The article summarizes the f...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872098/ https://www.ncbi.nlm.nih.gov/pubmed/29361736 http://dx.doi.org/10.3390/jfb9010012 |
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author | Vitetta, Luis Zhou, Joyce Manuel, Rachel Dal Forno, Serena Hall, Sean Rutolo, David |
author_facet | Vitetta, Luis Zhou, Joyce Manuel, Rachel Dal Forno, Serena Hall, Sean Rutolo, David |
author_sort | Vitetta, Luis |
collection | PubMed |
description | The administration of biological compounds that optimize health benefits is an ever-evolving therapeutic goal. Pharmaceutical and other adjunctive biological compounds have been administered via many different routes in order to produce a systemic pharmacological effect. The article summarizes the findings from an Australian comparative study in adults administered vitamin B(12) through different oral delivery platforms. A total of 16 subjects (9 males, 7 females) voluntarily partook in a comparative clinical study of five different vitamin B(12) formulations across a six-month period, completing 474 person-hours of cumulative contribution, that was equivalent to an n = 60 participation. A nanoparticle delivered vitamin B(12) through a NanoCelle platform was observed to be significantly (p < 0.05) better absorbed than all other dose equivalent platforms (i.e., tablets, emulsions, or liposomes) from baseline to 1, 3, and 6 h of the study period. The nanoparticle platform delivered vitamin B(12) demonstrated an enhanced and significant absorption profile as exemplified by rapid systemic detection (i.e., 1 h from baseline) when administered to the oro-buccal mucosa with no reports of any adverse events of toxicity. The nanoparticle formulation of methylcobalamin (1000 µg/dose in 0.3 mL volume) showed bioequivalence only with a chewable-dissolvable tablet that administered a five times higher dose of methylcobalamin (5000 µg) per tablet. This study has demonstrated that an active metabolite embedded in a functional biomaterial (NanoCelle) may constitute a drug delivery method that can better access the circulatory system. |
format | Online Article Text |
id | pubmed-5872098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58720982018-03-30 Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum Vitetta, Luis Zhou, Joyce Manuel, Rachel Dal Forno, Serena Hall, Sean Rutolo, David J Funct Biomater Article The administration of biological compounds that optimize health benefits is an ever-evolving therapeutic goal. Pharmaceutical and other adjunctive biological compounds have been administered via many different routes in order to produce a systemic pharmacological effect. The article summarizes the findings from an Australian comparative study in adults administered vitamin B(12) through different oral delivery platforms. A total of 16 subjects (9 males, 7 females) voluntarily partook in a comparative clinical study of five different vitamin B(12) formulations across a six-month period, completing 474 person-hours of cumulative contribution, that was equivalent to an n = 60 participation. A nanoparticle delivered vitamin B(12) through a NanoCelle platform was observed to be significantly (p < 0.05) better absorbed than all other dose equivalent platforms (i.e., tablets, emulsions, or liposomes) from baseline to 1, 3, and 6 h of the study period. The nanoparticle platform delivered vitamin B(12) demonstrated an enhanced and significant absorption profile as exemplified by rapid systemic detection (i.e., 1 h from baseline) when administered to the oro-buccal mucosa with no reports of any adverse events of toxicity. The nanoparticle formulation of methylcobalamin (1000 µg/dose in 0.3 mL volume) showed bioequivalence only with a chewable-dissolvable tablet that administered a five times higher dose of methylcobalamin (5000 µg) per tablet. This study has demonstrated that an active metabolite embedded in a functional biomaterial (NanoCelle) may constitute a drug delivery method that can better access the circulatory system. MDPI 2018-01-21 /pmc/articles/PMC5872098/ /pubmed/29361736 http://dx.doi.org/10.3390/jfb9010012 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vitetta, Luis Zhou, Joyce Manuel, Rachel Dal Forno, Serena Hall, Sean Rutolo, David Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum |
title | Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum |
title_full | Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum |
title_fullStr | Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum |
title_full_unstemmed | Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum |
title_short | Route and Type of Formulation Administered Influences the Absorption and Disposition of Vitamin B(12) Levels in Serum |
title_sort | route and type of formulation administered influences the absorption and disposition of vitamin b(12) levels in serum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5872098/ https://www.ncbi.nlm.nih.gov/pubmed/29361736 http://dx.doi.org/10.3390/jfb9010012 |
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