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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Online Access: | http://dx.doi.org/10.1080/10717544.2021.1889718 |
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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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