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明胶纳米涂层抑制无定形药物表面结晶。

Gelatin Nano-coating for Inhibiting Surface Crystallization of Amorphous Drugs.

机构信息

School of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin, 53705, USA.

Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, 53705, USA.

出版信息

Pharm Res. 2018 Jan 5;35(1):23. doi: 10.1007/s11095-017-2315-z.

Abstract

PURPOSE

Inhibit the fast surface crystallization of amorphous drugs with gelatin nano-coatings.

METHODS

The free surface of amorphous films of indomethacin or nifedipine was coated by a gelatin solution (type A or B) and dried. The coating's effect on surface crystallization was evaluated. Coating thickness was estimated from mass change after coating.

RESULTS

For indomethacin (weak acid, pK = 4.5), a gelatin coating of either type deposited at pH 5 and 10 inhibited its fast surface crystal growth. The coating thickness was 20 ± 10 nm. A gelatin coating deposited at pH 3, however, provided no protective effect. These results suggest that an effective gelatin coating does not require that the drug and the polymer have opposite charges. The ineffective pH 3 coating might reflect the poor wetting of indomethacin's neutral, hydrophobic surface by the coating solution. For nifedipine (weak base, pK = 2.6), a gelatin coating of either type deposited at pH 5 inhibited its fast surface crystal growth.

CONCLUSIONS

Gelatin nano-coatings can be conveniently applied to amorphous drugs from solution to inhibit fast surface crystallization. Unlike strong polyelectrolyte coatings, a protective gelatin coating does not require strict pairing of opposite charges. This could make gelatin coating a versatile, pharmaceutically acceptable coating for stabilizing amorphous drugs.

摘要

目的

用明胶纳米涂层抑制无定形药物的快速表面结晶。

方法

将吲哚美辛或硝苯地平的无定形薄膜的自由表面用明胶溶液(A 型或 B 型)涂覆并干燥。评估涂层对表面结晶的影响。通过涂层后的质量变化来估计涂层厚度。

结果

对于吲哚美辛(弱酸,pK=4.5),在 pH 5 和 10 下沉积的任何类型的明胶涂层都能抑制其快速表面晶体生长。涂层厚度为 20±10nm。然而,在 pH 3 下沉积的明胶涂层没有提供保护作用。这些结果表明,有效的明胶涂层并不要求药物和聚合物具有相反的电荷。无效的 pH 3 涂层可能反映了涂层溶液对吲哚美辛中性疏水面的不良润湿性。对于硝苯地平(弱碱,pK=2.6),在 pH 5 下沉积的任何类型的明胶涂层都能抑制其快速表面晶体生长。

结论

明胶纳米涂层可以方便地从溶液中应用于无定形药物,以抑制快速表面结晶。与强聚电解质涂层不同,保护性明胶涂层不需要严格配对相反的电荷。这使得明胶涂层成为一种通用的、可接受的稳定无定形药物的涂层。

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