Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals

Solid dosage forms of biopharmaceuticals such as therapeutic proteins could provide enhanced bioavailability, improved storage stability, as well as expanded alternatives to parenteral administration. Although numerous drying methods have been used for preparing dried protein powders, choosing a sui...

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Main Authors: Fakhrossadat Emami, Alireza Vatanara, Eun Ji Park, Dong Hee Na
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:Pharmaceutics
Subjects:
Online Access:http://www.mdpi.com/1999-4923/10/3/131
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spelling doaj-7d6429f0e0254ee2ac3a7bea57b0a4512020-11-24T22:49:52ZengMDPI AGPharmaceutics1999-49232018-08-0110313110.3390/pharmaceutics10030131pharmaceutics10030131Drying Technologies for the Stability and Bioavailability of BiopharmaceuticalsFakhrossadat Emami0Alireza Vatanara1Eun Ji Park2Dong Hee Na3College of Pharmacy, Tehran University of Medical Sciences, Tehran 1417614411, IranCollege of Pharmacy, Tehran University of Medical Sciences, Tehran 1417614411, IranCollege of Pharmacy, Chung-Ang University, Seoul 06974, KoreaCollege of Pharmacy, Chung-Ang University, Seoul 06974, KoreaSolid dosage forms of biopharmaceuticals such as therapeutic proteins could provide enhanced bioavailability, improved storage stability, as well as expanded alternatives to parenteral administration. Although numerous drying methods have been used for preparing dried protein powders, choosing a suitable drying technique remains a challenge. In this review, the most frequent drying methods, such as freeze drying, spray drying, spray freeze drying, and supercritical fluid drying, for improving the stability and bioavailability of therapeutic proteins, are discussed. These technologies can prepare protein formulations for different applications as they produce particles with different sizes and morphologies. Proper drying methods are chosen, and the critical process parameters are optimized based on the proposed route of drug administration and the required pharmacokinetics. In an optimized drying procedure, the screening of formulations according to their protein properties is performed to prepare a stable protein formulation for various delivery systems, including pulmonary, nasal, and sustained-release applications.http://www.mdpi.com/1999-4923/10/3/131biopharmaceuticalsdrying technologyprotein stabilitybioavailabilitypharmacokinetics
collection DOAJ
language English
format Article
sources DOAJ
author Fakhrossadat Emami
Alireza Vatanara
Eun Ji Park
Dong Hee Na
spellingShingle Fakhrossadat Emami
Alireza Vatanara
Eun Ji Park
Dong Hee Na
Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals
Pharmaceutics
biopharmaceuticals
drying technology
protein stability
bioavailability
pharmacokinetics
author_facet Fakhrossadat Emami
Alireza Vatanara
Eun Ji Park
Dong Hee Na
author_sort Fakhrossadat Emami
title Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals
title_short Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals
title_full Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals
title_fullStr Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals
title_full_unstemmed Drying Technologies for the Stability and Bioavailability of Biopharmaceuticals
title_sort drying technologies for the stability and bioavailability of biopharmaceuticals
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2018-08-01
description Solid dosage forms of biopharmaceuticals such as therapeutic proteins could provide enhanced bioavailability, improved storage stability, as well as expanded alternatives to parenteral administration. Although numerous drying methods have been used for preparing dried protein powders, choosing a suitable drying technique remains a challenge. In this review, the most frequent drying methods, such as freeze drying, spray drying, spray freeze drying, and supercritical fluid drying, for improving the stability and bioavailability of therapeutic proteins, are discussed. These technologies can prepare protein formulations for different applications as they produce particles with different sizes and morphologies. Proper drying methods are chosen, and the critical process parameters are optimized based on the proposed route of drug administration and the required pharmacokinetics. In an optimized drying procedure, the screening of formulations according to their protein properties is performed to prepare a stable protein formulation for various delivery systems, including pulmonary, nasal, and sustained-release applications.
topic biopharmaceuticals
drying technology
protein stability
bioavailability
pharmacokinetics
url http://www.mdpi.com/1999-4923/10/3/131
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AT alirezavatanara dryingtechnologiesforthestabilityandbioavailabilityofbiopharmaceuticals
AT eunjipark dryingtechnologiesforthestabilityandbioavailabilityofbiopharmaceuticals
AT dongheena dryingtechnologiesforthestabilityandbioavailabilityofbiopharmaceuticals
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