20 Molecular Weight ( M w ), and polar Surface Area (PSA) Collected from PubChem,
the Stability of Drug Microneedles and Cooled-Molten Drug Samples under Respective Storage Conditions, Melting Point ( T m ), and Glass Transition ( T g ) Were Verified by DSC Analysis, and Amorphous Drug Hygroscopicity Determined Experimentally by DVS Analysis" width="100%" height="100%">
Journal: Molecular Pharmaceutics
Article Title: Glassy Drug Microneedle Array Design: Drug Glass-Forming Ability and Stability
doi: 10.1021/acs.molpharmaceut.4c01067
Figure Lengend Snippet: Drug Candidates Investigated Including Their GFA Class Determined Experimentally Using DSC Methodology, 20 Molecular Weight ( M w ), and polar Surface Area (PSA) Collected from PubChem, a the Stability of Drug Microneedles and Cooled-Molten Drug Samples under Respective Storage Conditions, Melting Point ( T m ), and Glass Transition ( T g ) Were Verified by DSC Analysis, and Amorphous Drug Hygroscopicity Determined Experimentally by DVS Analysis
Article Snippet: Itraconazole (ITZ), zolmitriptan (ZMT), and 17-β-estradiol hemihydrate (E2) were purchased from Kemprotec (UK) Ltd.; indomethacin (IMN) was purchased from Sigma-Aldrich (Ireland) Ltd.; T-zero calorimetry pans were acquired from Waters TA Instruments Ireland (Dublin, Ireland); 1525L adhesive tape was obtained from 3 M, USA; master mold 7000-grade aluminum was provided by SMAE Engineering Workshop, Queen University Belfast (UK) to design a 14 × 14 microneedle array, 500 μm length/height, and 300 μm diameter base; SYLGARD 184 Silicone Elastomer Kit was purchased from Ellsworth Adhesives Limited (UK), and polydimethylsiloxane microneedle molds were manufactured according to the manufacturer’s instructions.
Techniques: Molecular Weight, Crystallization Assay