Method of making oral dosage forms
The present invention relates to a method of making an oral dosage form comprising the steps of reacting at least one cell penetrating peptide (CPP), purifying CPP-lipid conjugates, processing a lipid batch to obtain CPP-modified liposomes and incorporating a liposome lyophilisate into an oral dosage form. The present invention further relates to oral dosage forms and oral dosage forms for use in a therapeutic method.
1. A method of making an oral dosage form, comprising the steps of
a. reacting at least one cell penetrating peptide (CPP) with at least one first lipid to obtain CPP-lipid conjugates, wherein the first lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(succinyl) (sodium salt), and wherein the CPP-lipid conjugates have a molecular weight from 1,200 to 5,000 g/mol,
b. purifying the CPP-lipid conjugates to obtain a purified CPP-lipid conjugate composition,
c. preparing a lipid batch comprising at least
c1. a defined amount of the CPP-lipid conjugates and
c2. a defined amount of at least one non-CPP-conjugated second lipid, wherein the second lipid is different from the first lipid,
d. processing the lipid batch to obtain CPP-modified liposomes having a zeta potential of more than 2 mV and less than 10 mV when measured in a solution of 50 mM phosphate buffer (pH 7.4) at a concentration of 0.95 mg/ml,
e. lyophilizing the CPP-modified liposomes to obtain a liposome lyophilisate,
f. incorporating the liposome lyophilisate into an oral dosage form,
wherein the amount of non-conjugated first lipid in the purified CPP-lipid conjugate composition is less than 5 mol % relative to the total molar amount of CPP-lipid conjugates in said composition.
2. The method according to claim 1 , wherein the CPP is selected from linear or cyclized polyarginines, linear or cyclized penetratin, linear or cyclized TAT (transactivator of transcription)-peptide, linear or cyclized MAP (model amphiphatic peptide), linear or cyclized pVEC, linear or cyclized transportan, and linear or cyclized MPG, dimers thereof, and combinations thereof.
3. The method according to claim 1 , wherein the amount of CPP in the CPP-modified liposome is not more than 4 mol %, relative to the cumulative amount of first and second lipids in the liposome.
4. The method according to claim 1 , wherein purifying the CPP-lipid conjugates to obtain a purified CPP-lipid conjugate composition includes the step of
b1. separating CPP-lipid conjugates from non-conjugated first lipid, and
b2. optionally separating CPP-lipid conjugates from non-conjugated CPP and/or conjugates carrying more than one CPP.
5. The method according to claim 1 , wherein processing the lipid batch to obtain CPP-modified liposomes, includes high pressure homogenization, extrusion, ethanol injection and/or dual asymmetric centrifugation (DAC).
6. The method according to claim 1 , wherein the CPP is a cyclic peptide.
7. The method according to claim 1 , wherein the CPP-modified liposomes have a Z-average diameter in the range of from 50 nm to 250 nm.
8. The method according to claim 1 , wherein the step of lyophilizing the CPP-modified liposomes to obtain a liposome lyophilisate includes:
e1. preparing a mixture of the CPP-modified liposomes and at least one lyoprotector.
9. The method according to claim 8 , wherein the lyoprotector is present in the mixture in a ratio of from 0.01 to 2 g of lyoprotector per 1 gram of lipid.
10. An oral dosage form comprising CPP-modified liposomes, having
at least one CPP conjugated to a first lipid, wherein the first lipid is 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(succinyl) (sodium salt), and wherein the CPP-lipid conjugates have a molecular weight from 1,200 to 5,000 g/mol;
at least one non-CPP-conjugated second lipid, wherein the second lipid is different from the first lipid, and
at least one pharmaceutically active ingredient, wherein the CPP-modified liposomes have a Z-average diameter in the range of from 50 nm to 250 nm, and a positive zeta potential in the range of from >2 mV to <10 mV when measured in a solution of 50 mM phosphate buffer (pH 7.4) at a concentration of 0.95 mg/ml.
11. The oral dosage form according to claim 10 , obtainable by a method comprising the steps of
a. reacting at least one CPP with at least one first lipid to obtain CPP-lipid conjugates,
b. purifying the CPP-lipid conjugates to obtain a purified CPP-lipid conjugate composition,
c. preparing a lipid batch comprising at least
c1. a defined amount of the CPP-lipid conjugates and
c2. a defined amount of at least one non-CPP-conjugated second lipid,
d. processing the lipid batch to obtain CPP-modified liposomes having a zeta potential of more than 2 mV and less than 10 mV when measured in a solution of 50 mM phosphate buffer (pH 7.4) at a concentration of 0.95 mg/ml,
e. lyophilizing the CPP-modified liposomes to obtain a liposome lyophilisate,
f. incorporating the liposome lyophilisate into an oral dosage form,
wherein the amount of non-conjugated first lipid in the purified CPP-lipid conjugate composition is less than 5 mol % relative to the total molar amount of CPP-lipid conjugates in said composition.
12. The oral dosage form according to claim 10 , wherein the amount of non-conjugated first lipid in the CPP-modified liposomes is less than 5 mol %, relative to the total molar amount of CPP-lipid conjugates in the CPP-modified liposomes.
13. The oral dosage form according to claim 10 , wherein the amount of CPP in the CPP-modified liposomes does not exceed 4 mol %, relative to the cumulative amount of first and second lipids in the liposome.
14. The oral dosage form according to claim 10 , wherein
the dosage form is selected from a tablet, a capsule, a pill, a powder, a liquid, a granulate, a pellet, a thin film, an effervescent formulation, a paste, a lozenge, a chewing gum, a gel, a spray or a combination thereof, and/or
the oral dosage form is for use in a therapeutic method.
15. The method according to claim 1 , wherein the CPP-lipid conjugates have a molecular weight of about 1,500 to about 3,500 g/mol.
16. The method according to claim 1 , wherein CPP-lipid conjugates are separated from non-conjugated CPP and/or conjugates carrying more than one CPP in step b.
17. The method according to claim 1 , wherein the amount of tetraether lipids in the liposomes is less than 0.01 mol %.