JOURNAL OF THE CZECH PHARMACEUTICAL SOCIETY AND THE SLOVAK PHARMACEUTICAL SOCIETY

Čes. slov. farm. 1999, 48(6):287-290

Dissolution and Supersaturation Episodes of Nimodipine in the Aqueous Solutions of the Cyclodextrins a-CD, HP-a-CD, M-b-CD, and HP-g-CD

F. Kopecký1, B. Kopecká2, P. Kaclík1
1 Katedra fyzikálnej chémie liečiv Farmaceutickej fakulty Univerzity Komenského, Bratislava
2 Katedra farmaceutickej analýzy a nukleárnej farmácie Farmaceutickej fakulty UniverzityKomenského, Bratislava

The dissolution curves of the substance of the calcium antagonist nimodipine in aqueous solutions of four cyclodextrins were determined at ambient temperature in the course of 14 days. The used cyclodextrins were a-cyclodextrin (a-CD), hydroxypropyl-a-cyclodextrin (HP-a-CD), methyl-b-cyclodextrin (M-b-CD, random-methylated), and hydroxypropyl-g-cyclodextrin (HP-g-CD) and their respective concentrations were always 0.05 mol/l. According to the measured dissolution curves, M-b-CD in aqueous medium was a highly efficient solubiliser, capable to dissolve otherwise sparingly soluble nimodipine into a time-stable aqueous solution, with the saturated concentration of nimodipine 5.15x10-4 mol/l (21.5 mg/100 ml) under the given conditions. M-b-CD thus appeared to be a more efficient solubiliser than the previously studied HP-b-CD. The solubilising power of HP-a-CD and HP-g-CD was much lower and a-CD practically did not improve long-term solubility of nimodipine in water. However, in the presence of a-CD, HP-a-CD, and HP-g-CD, respectively, repeated shortterm episodes of formation of supersaturated solutions of nimodipine were observedon the dissolution curves, characterised by peaks of nimodipine concentration. Similar supersaturation episodes were previously observed in the presence of HP-b-CD. Since the supersaturation caused by cyclodextrins reportedly substantially improved the biological availability of some drugs, the above-mentioned cyclodextrins, and especially natural a-CD, could be useful for the enhancement of the low availability of nimodipine from solid oral drug preparations.

Keywords: nimodipine; calcium antagonist; cyclodextrins; solubilisation; supersaturated solutions

Published: June 1, 1999  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Kopecký F, Kopecká B, Kaclík P. Dissolution and Supersaturation Episodes of Nimodipine in the Aqueous Solutions of the Cyclodextrins a-CD, HP-a-CD, M-b-CD, and HP-g-CD. Čes. slov. farm. 1999;48(6):287-290.
Download citation




Czech and Slovak Pharmacy

Madam, Sir,
please be aware that the website on which you intend to enter, not the general public because it contains technical information about medicines, including advertisements relating to medicinal products. This information and communication professionals are solely under §2 of the Act n.40/1995 Coll. Is active persons authorized to prescribe or supply (hereinafter expert).
Take note that if you are not an expert, you run the risk of danger to their health or the health of other persons, if you the obtained information improperly understood or interpreted, and especially advertising which may be part of this site, or whether you used it for self-diagnosis or medical treatment, whether in relation to each other in person or in relation to others.

I declare:

  1. that I have met the above instruction
  2. I'm an expert within the meaning of the Act n.40/1995 Coll. the regulation of advertising, as amended, and I am aware of the risks that would be a person other than the expert input to these sites exhibited


No

Yes

If your statement is not true, please be aware
that brings the risk of danger to their health or the health of others.