The present work investigated the solid state change of 4 acyclovir polymorphs when ground at room temperature (Method A) and under cryo-grinding in the presence of liquid nitrogen (Method B). Modifications in particle size and shape (evaluated by scanning electron microscopy) and in the water content (evaluated by thermal analysis) were related to transitions at the solid state, as confirmed by X-ray powder diffractometry. Anhydrous Form I was stable under grinding by both Methods A and B. The anhydrous Form II was stable during grinding under Method A, whereas it was progressively converted to the hydrate Form V during grinding under Method B. The hydrate Form V was stable under Method A, whereas it was converted to the anhydrous Form I after 15 min and then to the hydrate Form VI after 45 min of grinding. The hydrate Form VI proved to be stable under grinding by both Methods A and B. Thus, Form I and VI were the only forms that yielded a sizeable decrease in particle size under grinding, with a consequent increase in particle dissolution rate, while maintaining solid state physicochemical stability. Form I treated under Method B grinding gave the best dissolution rate. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
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Chungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South KoreaChungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South Korea
Park, Hee Jun
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Kim, Min-Soo
Kim, Jeong-Soo
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Chungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South KoreaChungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South Korea
Kim, Jeong-Soo
Cho, Wonkyung
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Chungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South KoreaChungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South Korea
Cho, Wonkyung
Park, Junsung
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Chungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South KoreaChungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South Korea
Park, Junsung
Cha, Kwang-Ho
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Chungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South KoreaChungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South Korea
Cha, Kwang-Ho
Kang, Young-Shin
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Chungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South KoreaChungnam Natl Univ, Coll Pharm, Ctr Nanotechnol Based New Drug Dosage Form, Taejon 305764, South Korea
机构:
Toho Univ, Fac Sci, Chiba 2748510, Japan
Toho Univ, Res Ctr Mat Integrated Properties, Chiba 2748510, JapanToho Univ, Fac Sci, Chiba 2748510, Japan
Ichimura, Kunihiro
Aoki, Ken'ichi
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Toho Univ, Fac Sci, Chiba 2748510, Japan
Toho Univ, Res Ctr Mat Integrated Properties, Chiba 2748510, JapanToho Univ, Fac Sci, Chiba 2748510, Japan
Aoki, Ken'ichi
Akiyama, Haruhisa
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Natl Inst Adv Ind Sci & Technol, Nanotechnol Res Inst, Tsukuba, Ibaraki 3058565, JapanToho Univ, Fac Sci, Chiba 2748510, Japan
Akiyama, Haruhisa
Horiuchi, Shin
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Natl Inst Adv Ind Sci & Technol, Nanotechnol Res Inst, Tsukuba, Ibaraki 3058565, JapanToho Univ, Fac Sci, Chiba 2748510, Japan
Horiuchi, Shin
Horie, Shinji
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Toda Kogyo Corp, R&D Ctr, Hiroshima 7390652, JapanToho Univ, Fac Sci, Chiba 2748510, Japan
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Univ Helsinki, Fac Pharm, Div Pharmaceut Technol, FIN-00014 Helsinki, FinlandUniv Helsinki, Fac Pharm, Div Pharmaceut Technol, FIN-00014 Helsinki, Finland