Erratum to To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations [Colloids Surf. B: Biointerf., (2010), 76, 170-178]

Al-Hamidi H.; Edwards A.A.; Mohammad M.A.; Nokhodchi A.

首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Erratum to To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations [Colloids Surf. B: Biointerf., (2010), 76, 170-178]

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Erratum to To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations [Colloids Surf. B: Biointerf., (2010), 76, 170-178]

机译：勘误以提高水溶性差的药物的溶出度：盐酸氨基葡萄糖作为固体分散体制剂中的潜在载体[胶体冲浪。 B：Biointerf。（2010），76，170-178]

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《Colloids and Surfaces, B. Biointerfaces》 |2010年第2期|共1页
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Al-Hamidi H.; Edwards A.A.; Mohammad M.A.; Nokhodchi A.;
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中图分类胶体化学（分散体系的物理化学）;
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1. Erratum to To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations [Colloids Surf. B: Biointerf., (2010), 76, 170-178] [J] . Al-Hamidi H., Edwards A.A., Mohammad M.A., Colloids and Surfaces, B. Biointerfaces . 2010,第2期

机译：勘误以提高水溶性差的药物的溶出度：盐酸氨基葡萄糖作为固体分散体制剂中的潜在载体[胶体冲浪。 B：Biointerf。（2010），76，170-178]
2. The dissolution enhancement of piroxicam in its physical mixtures and solid dispersion formulations using gluconolactone and glucosamine hydrochloride as potential carriers [J] . Al-Hamidi Hiba, Obeidat Wasfy M., Nokhodchi Ali Pharmaceutical development and technology . 2015,第1a8期

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3. Sodium alginate as a potential carrier in solid dispersion formulations to enhance dissolution rate and apparent water solubility of BCS II drugs [J] . Amarante Borba Paola Aline, Pinotti Mariha, Maduro de Campos Carlos Eduardo, Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides . 2016,第Null期

机译：海藻酸钠作为固体分散体制剂中的潜在载体，可提高BCS II药物的溶出度和表观水溶性
4. Development of Clinical Dosage Forms for a Poorly Water-Soluble Drug II: Comparative Evaluation of Solid Dispersion, Solid Microemulsion Preconcentrate and Lipid-based Formulations [C] . Rose-Marie Dannenfelser, Handan He, Ping Li, Controlled Release Society Annual Meeting and Exposition . 2007

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5. Investigation of Amorphous Solid Dispersions for Solubility Enhancement of Poorly Water-Soluble Drugs: Understanding the Effect of Material Properties on Amorphous Drug Crystallization and the Impact on Formulation Performance [D] . Ojo, Andrew Olutoye. 2021

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6. Potential of solid dispersions to enhance solubility bioavailability and therapeutic efficacy of poorly water-soluble drugs: newer formulation techniques current marketed scenario and patents [O] . Sultan Alshehri, Syed Sarim Imam, Afzal Hussain, 2020

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7. Formulation and enhancement of dissolution rate of poorly aqueous soluble drug Aceclofenac by solid dispersion method: In vitro study [O] . Neupane Sumana, Thapa Chhitij 2020

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Erratum to To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations [Colloids Surf. B: Biointerf., (2010), 76, 170-178]

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