TY - JOUR
T1 - Innovative Drying Technologies for Biopharmaceuticals
AU - Sharma, Ashutosh
AU - Khamar, Dikshitkumar
AU - Cullen, Sean
AU - Hayden, Ambrose
AU - Hughes, Helen
N1 - Funding Information:
The authors acknowledge funding received from Waterford Institute of Technology – Sanofi Waterford Co-fund PhD Scholarship Program (Ashutosh Sharma) and the Irish Research Council – Enterprise Partnership Scheme (Project ID: EPSPG/2020/56). The authors also acknowledge Robert Turok at SPX Flow Inc. for his valuable suggestions on spray-drying in the manuscript.
Funding Information:
The authors acknowledge funding received from Waterford Institute of Technology ? Sanofi Waterford Co-fund PhD Scholarship Program (Ashutosh Sharma) and the Irish Research Council ? Enterprise Partnership Scheme (Project ID: EPSPG/2020/56). The authors also acknowledge Robert Turok at SPX Flow Inc. for his valuable suggestions on spray-drying in the manuscript.
Publisher Copyright:
© 2021 The Author(s)
PY - 2021/11/20
Y1 - 2021/11/20
N2 - In the past two decades, biopharmaceuticals have been a breakthrough in improving the quality of lives of patients with various cancers, autoimmune, genetic disorders etc. With the growing demand of biopharmaceuticals, the need for reducing manufacturing costs is essential without compromising on the safety, quality, and efficacy of products. Batch Freeze-drying is the primary commercial means of manufacturing solid biopharmaceuticals. However, Freeze-drying is an economically unfriendly means of production with long production cycles, high energy consumption and heavy capital investment, resulting in high overall costs. This review compiles some potential, innovative drying technologies that have not gained popularity for manufacturing parenteral biopharmaceuticals. Some of these technologies such as Spin-freeze-drying, Spray-drying, Lynfinity® Technology etc. offer a paradigm shift towards continuous manufacturing, whereas PRINT® Technology and MicroglassificationTM allow controlled dry particle characteristics. Also, some of these drying technologies can be easily scaled-up with reduced requirement for different validation processes. The inclusion of Process Analytical Technology (PAT) and offline characterization techniques in tandem can provide additional information on the Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs) during biopharmaceutical processing. These processing technologies can be envisaged to increase the manufacturing capacity for biopharmaceutical products at reduced costs.
AB - In the past two decades, biopharmaceuticals have been a breakthrough in improving the quality of lives of patients with various cancers, autoimmune, genetic disorders etc. With the growing demand of biopharmaceuticals, the need for reducing manufacturing costs is essential without compromising on the safety, quality, and efficacy of products. Batch Freeze-drying is the primary commercial means of manufacturing solid biopharmaceuticals. However, Freeze-drying is an economically unfriendly means of production with long production cycles, high energy consumption and heavy capital investment, resulting in high overall costs. This review compiles some potential, innovative drying technologies that have not gained popularity for manufacturing parenteral biopharmaceuticals. Some of these technologies such as Spin-freeze-drying, Spray-drying, Lynfinity® Technology etc. offer a paradigm shift towards continuous manufacturing, whereas PRINT® Technology and MicroglassificationTM allow controlled dry particle characteristics. Also, some of these drying technologies can be easily scaled-up with reduced requirement for different validation processes. The inclusion of Process Analytical Technology (PAT) and offline characterization techniques in tandem can provide additional information on the Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs) during biopharmaceutical processing. These processing technologies can be envisaged to increase the manufacturing capacity for biopharmaceutical products at reduced costs.
KW - Biopharmaceuticals
KW - Characterization Techniques
KW - Drying Technologies
KW - Formulation
KW - Process Analytical Technology
UR - http://www.scopus.com/inward/record.url?scp=85116524959&partnerID=8YFLogxK
U2 - 10.1016/j.ijpharm.2021.121115
DO - 10.1016/j.ijpharm.2021.121115
M3 - Review article
C2 - 34547393
AN - SCOPUS:85116524959
SN - 0378-5173
VL - 609
JO - International Journal of Pharmaceutics
JF - International Journal of Pharmaceutics
M1 - 121115
ER -