<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mutukuri TT</submitter><funding>NIAID NIH HHS</funding><pagination>40-50</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9772299</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>112(1)</volume><pubmed_abstract>This study examined physical stability of spray freeze dried (SFD) bovine serum albumin (BSA) solids produced using the radio frequency (RF)-assisted drying technique. BSA formulations were prepared with varying concentrations of trehalose and mannitol, using an excipient-free formulation as control. These formulations were produced using either traditional ultrasonic spray freeze drying (SFD) or RF-assisted ultrasonic spray freeze drying (RFSFD). The dried formulations were then characterized using Karl Fischer moisture content measurement, powder X-ray diffraction (PXRD), size exclusion chromatography (SEC), and solid-state hydrogen/deuterium exchange with mass spectrometry (ssHDX-MS). Moisture content did not have a good correlation with the physical stability of the formulations measur</pubmed_abstract><journal>Journal of pharmaceutical sciences</journal><pubmed_title>Radio Frequency - Assisted Ultrasonic Spray Freeze Drying for Pharmaceutical Protein Solids.</pubmed_title><pmcid>PMC9772299</pmcid><funding_grant_id>R01 AI146160</funding_grant_id><pubmed_authors>Strongrich AD</pubmed_authors><pubmed_authors>Peroulis D</pubmed_authors><pubmed_authors>Zhou QT</pubmed_authors><pubmed_authors>Mutukuri TT</pubmed_authors><pubmed_authors>Darwish A</pubmed_authors><pubmed_authors>Alexeenko A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Radio Frequency - Assisted Ultrasonic Spray Freeze Drying for Pharmaceutical Protein Solids.</name><description>This study examined physical stability of spray freeze dried (SFD) bovine serum albumin (BSA) solids produced using the radio frequency (RF)-assisted drying technique. BSA formulations were prepared with varying concentrations of trehalose and mannitol, using an excipient-free formulation as control. These formulations were produced using either traditional ultrasonic spray freeze drying (SFD) or RF-assisted ultrasonic spray freeze drying (RFSFD). The dried formulations were then characterized using Karl Fischer moisture content measurement, powder X-ray diffraction (PXRD), size exclusion chromatography (SEC), and solid-state hydrogen/deuterium exchange with mass spectrometry (ssHDX-MS). Moisture content did not have a good correlation with the physical stability of the formulations measur</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-26T07:52:44.168Z</modification><creation>2025-04-06T12:28:06.627Z</creation></dates><accession>S-EPMC9772299</accession><cross_references><pubmed>36181875</pubmed><doi>10.1016/j.xphs.2022.09.024</doi></cross_references></HashMap>