Coated pellets
Coated pellets which comprise an active pharmaceutical ingredient that is poorly soluble in water, release at least 80% of the active ingredient under in vitro conditions in phosphate buffer at pH 5.0 after 30 minutes and are bioequivalent to a liquid formulation of the active ingredient under in vitro fed status test conditions and/or are coated with a composition, which includes a lipophilic component (A) and a hydrogel former (B), wherein the pure lipophilic component (A) has (i) an HLB value of ≦5, and/or (ii) a melting range of ≧60° C., and/or (iii) a solidification range Δ of less than 35° C., and/or (iv) a density of ≧0.80 g cm −3 .
1. Coated pellets, which comprise an active pharmaceutical ingredient that has a solubility of at most 20 mg ml −1 in pure water at 23° C.;
release at least 80% of said active ingredient under in vitro conditions in phosphate buffer at pH 5.0 after 30 minutes, and
are coated with a composition consisting of a wax (A) and a hydrogel former (B);
wherein said wax (A) has at least one characteristic selected from the group consisting of:
(i) an HLB value of ≦5;
(ii) a melting range of ≧60° C.;
(iii) a solidification range Δ of less than 35° C., and
(iv) a density of ≧0.80 g cm −3 ; and
wherein the hydrogel former (B) is selected from the group consisting of carbomer, guar gum, L-HPC, and xanthan gum.
2. The pellets according to claim 1 , wherein said pellets are bioequivalent to a juice formulation of said active ingredient under in vivo fasted status test conditions.
3. The pellets according to claim 1 , wherein said pellets are extruded pellets.
4. The pellets according to claim 1 , wherein said pellets have a core containing at least one substance selected from the group consisting of sugar esters, sulfated polysaccharides and Ca 3 (PO 4 ) 2 .
5. The pellets according to claim 4 , wherein said core contains carrageenan.
6. The pellets according to claim 1 , wherein said hydrogel former (B) comprises from 2.5 to 50% by weight of the coating composition.
7. The pellets according to claim 1 , wherein the coating composition is applied in a quantity, which corresponds to a weight increase of 1 to 50% g/g in relation to the weight of the uncoated pellets.
8. The pellets according to claim 1 , wherein said pellets release at least 90% of the active ingredient under in vitro conditions in phosphate buffer at pH 5.0 after 30 minutes.
9. The pellets according to claim 1 , wherein said pellets exhibit an active ingredient release profile which is substantially unchanged before and after storage for 1 month at 30° C. and 60% relative humidity.
10. The pellets according to claim 1 , wherein said active ingredient is an antibiotic which exhibits bacteriostatic, bactericidal or bacteriolytic activity against gram + bacteria or against gram − bacteria or against both gram + and gram − bacteria.
11. The pellets according to claim 10 , wherein the antibiotic is selected from the group consisting of cell-wall synthesis inhibitors, inhibitors of protein biosynthesis on ribosomes, gyrase inhibitors, folic acid antagonists, and inhibitors of bacterial RNA polymerase.
12. The pellets according to claim 10 , wherein said antibiotic is selected from the group consisting of tetracyclines, amphenicols, β-lactam antibiotics, penicillins, sulfonamides, trimethoprim, macrolides, lincosamides, streptogramins, aminoglycoside antibiotics, and quinolones.
13. The pellets according to claim 12 , wherein said antibiotic is selected from the group consisting of second generation cephalosporins, third generation cephalosporins, and macrolides.
14. The pellets according to claim 12 , wherein said antibiotic is selected from the group consisting of azithromycin, cefpodoxime, cefpodoximproxetil, cefuroxime, cerfuroximaxetil, cefixime, cefdinir and clarithromycin.
15. An orally administrable pharmaceutical dosage form comprising the coated pellets according to claim 1 .
16. A pharmaceutical dosage form according to claim 15 , wherein after oral administration a maximum plasma concentration C max of the active ingredient is achieved after a t max in the range of 1 hour to 8 hours.
17. A drinking straw containing the pellets according to claim 1 , such that ingestion of a liquid through said straw by a subject results in ingestion of said active agent.
18. A coating composition for a pharmaceutical composition, said coating composition consisting of a wax (A) and a hydrogel former (B);
wherein said wax (A) has at least one characteristic selected from the group consisting of:
(v) an HLB value of ≦5;
(vi) a melting range of ≧60° C.;
(vii) a solidification range Δ of less than 35° C., and
(viii) a density of ≧0.80 g cm −3 ; and
wherein the hydrogel former (B) is selected from the group consisting of carbomer, guar gum, L-HPC, and xanthan gum.