Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Clarithromycin | HCID 84029 | — |
| Edukt | Delta-Tocopherol | HCID 92094 | — |
| Edukt | Glyceryl 1-monooctanoate | HCID 3033877 | — |
| Edukt | HCID 44428588 | HCID 44428588 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 44428588 | HCID 44428588 | — |
| Produkt | Tocol, (2R)- | HCID 58866062 | — |
Reaktionsschritte
Clarithromycin was obtained as the free base from Wockhardt (Delhi, India). Vitamin E Succinate (VESA) was obtained from Eastman (Freeport Tenn.). Capmul® MCM was obtained from Abitec (Janesville Wis.); Poloxamer® 407 (Pluronic® F-127) from BASF (Parsippany N.J.); PEG-400 from Spectrum Chemicals (Gardenia Calif.), and d-δ-tocopherol from Sigma Chemicals (St Louis MO). An oil phase consisting of d-δ-tocopherol and Capmul MCM was prepared using 2 parts of δ-tocopherol. Surfactant and clarithromycin were then added as shown in the table below. Dry ethanol was used to dissolve the components at 70° C. and the ethanol was then removed under vacuum. A clear amber oil resulted, but upon cooling, oblong, “casket-lid” crystals of clarithromycin were observed. A tocol-soluble ion pair of this compound was then produced by addition of a stoichiometric equivalent of Vitamin E succinate (VESA) as the free acid. On re-dissolution in ethanol and cooling no crystals formed. The clarithromycin was now sufficiently soluble in the tocopherol oil to allow subsequent preparation of the emulsion. The oil was then re-heated to 45° C. and degassed immediately prior to emulsification as described below.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06479540B1 |
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| Quelldatensatz | uspto-grants-2002_11 |
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| ORD ID | ord-4560e163006149e48bfb73577bd2881e |
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| Quellennotiz | uspto-grants-2002_11 |
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