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Pharmaceutical Cyclodextrin

Hydroxypropyl-beta-cyclodextrin

Hydroxypropyl-beta-cyclodextrin

The introduction of hydroxypropyl breaks the intramolecular cyclic hydrogen bonding of betacyclodextrin, which overcomes the main disadvantage of poor water solubility of betacyclodextrin while maintaining the cyclodextrin cavity.

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Betadex sulfobutyl ether sodium

Betadex sulfobutyl ether sodium

Normally its elimination from the kidneys is rapid and complete after administration. In vitro experiments and in vivo acute, subacute and chronic toxicity studies provide safe data and approved for use in human pharmaceutical preparations.

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Hydroxypropyl gamma cyclodextrin

Hydroxypropyl gamma cyclodextrin

Hydroxypropyl Gamma Cyclodextrin solubilizes large molecules, such as cholesterol, for use in cell culture. Hydroxypropyl gamma cyclodextrin is similar to betacyclodextrin but solubilizes larger molecules.

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Oral grade hydroxypropyl betacyclodextrin

Oral grade hydroxypropyl betacyclodextrin

The introduction of hydroxypropyl (2-hydroxypropyl) destroys the hydrogen bonds within the ring of β-cyclodextrin, which not only retains the cyclodextrin cavity, but also overcomes the main shortcoming of poor water solubility of β-cyclodextrin.

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Injection grade hydroxypropyl betacyclodextrin

Injection grade hydroxypropyl betacyclodextrin

The introduction of hydroxypropyl (2-hydroxypropyl) destroys the hydrogen bonds within the ring of β-cyclodextrin, which not only retains the cyclodextrin cavity, but also overcomes the main shortcoming of poor water solubility of β-cyclodextrin.

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