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Improving blend content uniformity via dry particle coating of micronized drug powders.
Eur J Pharm Sci. 2017 Jun 15; 104:344-355.EJ

Abstract

Content uniformity of low dose blends with fine active pharmaceutical ingredients (API) is adversely impacted due to API agglomeration caused by high powder cohesion. Dry coating using high-intensity vibratory mixing is employed to reduce API cohesion and granular Bond number as well as agglomeration as predicted by contact models, hence improve blend content uniformity (CU). Micronized acetaminophen (mAPAP) (~10μm), a model API, was dry coated with nano-silica R972P (20nm), and mixed with Avicel 102. The amount of silica was varied from 0 to 2.74wt%, corresponding to theoretical surface area coverage (SAC) from 0 to 100% respectively. Bulk density, unconfined yield strength, and dispersive surface energy results indicated dry coating with 0.27 to 1.0wt% silica was adequate for API property enhancement; further corroborated by improved CU for 5wt% API blends. Excellent CU was achieved for 3, 5 and 10wt% API loaded blends, where 30min of mixing was found to be acceptable for all three. The CU with dry coated mAPAP was significantly lower and within the acceptable range as compared to control blends without silica, as well as those with silica added during blending. Sieving of mAPAP illustrated the reduction in mAPAP agglomeration, necessary for improved CU after dry coating, corroborating model based predictions. Compared to theoretical predictions, actual CU was higher unless API agglomerate size distribution obtained via sieving was taken into account. Overall, cohesion reduction by dry coating is shown as a promising approach for improving content uniformity of cohesive API blends.

Authors+Show Affiliations

Otto H. York Department of Chemical, Biological, and Pharmaceutical Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.Otto H. York Department of Chemical, Biological, and Pharmaceutical Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.Otto H. York Department of Chemical, Biological, and Pharmaceutical Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.Otto H. York Department of Chemical, Biological, and Pharmaceutical Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA.Otto H. York Department of Chemical, Biological, and Pharmaceutical Engineering, New Jersey Institute of Technology, Newark, NJ 07102, USA. Electronic address: dave@njit.edu.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28435077

Citation

Huang, Zhonghui, et al. "Improving Blend Content Uniformity Via Dry Particle Coating of Micronized Drug Powders." European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences, vol. 104, 2017, pp. 344-355.
Huang Z, Xiong W, Kunnath K, et al. Improving blend content uniformity via dry particle coating of micronized drug powders. Eur J Pharm Sci. 2017;104:344-355.
Huang, Z., Xiong, W., Kunnath, K., Bhaumik, S., & Davé, R. N. (2017). Improving blend content uniformity via dry particle coating of micronized drug powders. European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences, 104, 344-355. https://doi.org/10.1016/j.ejps.2017.04.012
Huang Z, et al. Improving Blend Content Uniformity Via Dry Particle Coating of Micronized Drug Powders. Eur J Pharm Sci. 2017 Jun 15;104:344-355. PubMed PMID: 28435077.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Improving blend content uniformity via dry particle coating of micronized drug powders. AU - Huang,Zhonghui, AU - Xiong,Wannan, AU - Kunnath,Kuriakose, AU - Bhaumik,Sayani, AU - Davé,Rajesh N, Y1 - 2017/04/20/ PY - 2016/11/08/received PY - 2017/03/11/revised PY - 2017/04/17/accepted PY - 2017/4/25/pubmed PY - 2018/4/4/medline PY - 2017/4/25/entrez KW - Cohesive API powder KW - Content uniformity KW - Dry coating KW - Granular Bond number KW - Low dose blends SP - 344 EP - 355 JF - European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences JO - Eur J Pharm Sci VL - 104 N2 - Content uniformity of low dose blends with fine active pharmaceutical ingredients (API) is adversely impacted due to API agglomeration caused by high powder cohesion. Dry coating using high-intensity vibratory mixing is employed to reduce API cohesion and granular Bond number as well as agglomeration as predicted by contact models, hence improve blend content uniformity (CU). Micronized acetaminophen (mAPAP) (~10μm), a model API, was dry coated with nano-silica R972P (20nm), and mixed with Avicel 102. The amount of silica was varied from 0 to 2.74wt%, corresponding to theoretical surface area coverage (SAC) from 0 to 100% respectively. Bulk density, unconfined yield strength, and dispersive surface energy results indicated dry coating with 0.27 to 1.0wt% silica was adequate for API property enhancement; further corroborated by improved CU for 5wt% API blends. Excellent CU was achieved for 3, 5 and 10wt% API loaded blends, where 30min of mixing was found to be acceptable for all three. The CU with dry coated mAPAP was significantly lower and within the acceptable range as compared to control blends without silica, as well as those with silica added during blending. Sieving of mAPAP illustrated the reduction in mAPAP agglomeration, necessary for improved CU after dry coating, corroborating model based predictions. Compared to theoretical predictions, actual CU was higher unless API agglomerate size distribution obtained via sieving was taken into account. Overall, cohesion reduction by dry coating is shown as a promising approach for improving content uniformity of cohesive API blends. SN - 1879-0720 UR - https://www.unboundmedicine.com/medline/citation/28435077/Improving_blend_content_uniformity_via_dry_particle_coating_of_micronized_drug_powders_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0928-0987(17)30206-3 DB - PRIME DP - Unbound Medicine ER -