Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)

For efficient intranasal transport of parathyroid hormone (1-34) [PTH(1-34)], there is a great medical need to investigate permeation enhancers for intranasal formulations. In this study, the development of PTH(1-34) intranasal formulations was conducted. Based on conformation and chemical stability...

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Main Authors: Dan Wang, Yimeng Du, Wenpeng Zhang, Xiaolu Han, Hui Zhang, Zengming Wang, Nan Liu, Meng Li, Xiang Gao, Xiaomei Zhuang, Jing Gao, Aiping Zheng
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Drug Delivery
Subjects:
Online Access:http://dx.doi.org/10.1080/10717544.2021.1889718
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spelling doaj-cd9275ada7ba4262b46e9288bb8648472021-03-18T15:12:46ZengTaylor & Francis GroupDrug Delivery1071-75441521-04642021-01-0128148749810.1080/10717544.2021.18897181889718Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)Dan Wang0Yimeng Du1Wenpeng Zhang2Xiaolu Han3Hui Zhang4Zengming Wang5Nan Liu6Meng Li7Xiang Gao8Xiaomei Zhuang9Jing Gao10Aiping Zheng11State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyState Key Laboratory of Toxicology and Medical Countermeasures, Beijing Institute of Pharmacology and ToxicologyFor efficient intranasal transport of parathyroid hormone (1-34) [PTH(1-34)], there is a great medical need to investigate permeation enhancers for intranasal formulations. In this study, the development of PTH(1-34) intranasal formulations was conducted. Based on conformation and chemical stability studies, the most preferable aqueous environment was determined to be 0.008 M acetate buffer solution (ABS). Subsequently, citric acid and Kolliphor® HS·15 were compared as permeation enhancers. The mechanisms of action of citric acid and Kolliphor® HS·15 were investigated using an in vitro model of nasal mucosa, and Kolliphor® HS·15 led to higher permeability of fluorescein isothiocyanate-labeled PTH(1-34) (FITC-PTH) by enhancing both the transcellular and paracellular routes. Moreover, citric acid showed severe mucosal toxicity resulting in cilia shedding, while Kolliphor® HS·15 did not cause obvious mucosa damage. Finally, Kolliphor® HS·15 was studied as a permeation enhancer using a liquid chromatography tandem mass spectrometry (LC-MS/MS) method. The results showed that 5% and 10% Kolliphor® HS·15 increased the bioavailability of PTH(1-34) to 14.76% and 30.87%, respectively. In conclusion, an effective and biosafe PTH(1-34) intranasal formulation was developed by using 10% Kolliphor® HS·15 as a permeation enhancer. Intranasal formulations with higher concentrations of Kolliphor® HS·15 for higher bioavailability of PTH(1-34) could be further researched.http://dx.doi.org/10.1080/10717544.2021.1889718parathyroid hormone (1-34)intranasal formulationpermeation enhancermucosal toxicitypharmacokinetics
collection DOAJ
language English
format Article
sources DOAJ
author Dan Wang
Yimeng Du
Wenpeng Zhang
Xiaolu Han
Hui Zhang
Zengming Wang
Nan Liu
Meng Li
Xiang Gao
Xiaomei Zhuang
Jing Gao
Aiping Zheng
spellingShingle Dan Wang
Yimeng Du
Wenpeng Zhang
Xiaolu Han
Hui Zhang
Zengming Wang
Nan Liu
Meng Li
Xiang Gao
Xiaomei Zhuang
Jing Gao
Aiping Zheng
Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
Drug Delivery
parathyroid hormone (1-34)
intranasal formulation
permeation enhancer
mucosal toxicity
pharmacokinetics
author_facet Dan Wang
Yimeng Du
Wenpeng Zhang
Xiaolu Han
Hui Zhang
Zengming Wang
Nan Liu
Meng Li
Xiang Gao
Xiaomei Zhuang
Jing Gao
Aiping Zheng
author_sort Dan Wang
title Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
title_short Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
title_full Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
title_fullStr Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
title_full_unstemmed Development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
title_sort development and in vivo evaluation of intranasal formulations of parathyroid hormone (1-34)
publisher Taylor & Francis Group
series Drug Delivery
issn 1071-7544
1521-0464
publishDate 2021-01-01
description For efficient intranasal transport of parathyroid hormone (1-34) [PTH(1-34)], there is a great medical need to investigate permeation enhancers for intranasal formulations. In this study, the development of PTH(1-34) intranasal formulations was conducted. Based on conformation and chemical stability studies, the most preferable aqueous environment was determined to be 0.008 M acetate buffer solution (ABS). Subsequently, citric acid and Kolliphor® HS·15 were compared as permeation enhancers. The mechanisms of action of citric acid and Kolliphor® HS·15 were investigated using an in vitro model of nasal mucosa, and Kolliphor® HS·15 led to higher permeability of fluorescein isothiocyanate-labeled PTH(1-34) (FITC-PTH) by enhancing both the transcellular and paracellular routes. Moreover, citric acid showed severe mucosal toxicity resulting in cilia shedding, while Kolliphor® HS·15 did not cause obvious mucosa damage. Finally, Kolliphor® HS·15 was studied as a permeation enhancer using a liquid chromatography tandem mass spectrometry (LC-MS/MS) method. The results showed that 5% and 10% Kolliphor® HS·15 increased the bioavailability of PTH(1-34) to 14.76% and 30.87%, respectively. In conclusion, an effective and biosafe PTH(1-34) intranasal formulation was developed by using 10% Kolliphor® HS·15 as a permeation enhancer. Intranasal formulations with higher concentrations of Kolliphor® HS·15 for higher bioavailability of PTH(1-34) could be further researched.
topic parathyroid hormone (1-34)
intranasal formulation
permeation enhancer
mucosal toxicity
pharmacokinetics
url http://dx.doi.org/10.1080/10717544.2021.1889718
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