Processes for the preparation of pharmaceutical compositions containing bromocriptine having high stability and related products
First Claim
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1. A method for the preparation of a pharmaceutical composition in tablet or capsule form containing the active ingredient bromocriptine base or bromocriptine salified with organic or inorganic acids, which method comprises the following steps:
- (a) dissolving the active ingredient in a solvent or mixture of solvents capable of producing a solution having a concentration of active ingredient greater than about 10%, said solvent being selected from ethyl and isopropyl alcohol, acetone, ethyl acetate, chloroform, methylene chloride, water and carbon tetrachloride;
(b) using the resultant solution to wet an excipient, or mixture of excipients, insoluble in said solution but subject to the swelling action thereof, said excipient being selected from cross-linked polyvinylpyrrolidone, cross-linked sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, alginic acid and salts thereof, starch and derivatives thereof and ion exchange resins, whereby an expanded excipient is obtained;
(c) drying said expanded excipient to produce an active ingredient-bearing excipient product having a residual moisture content of less than 1% and subjecting said product to separation; and
(d) compressing said product into tablets or distributing it into capsules.
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Abstract
Processes for the preparation of bromocriptine tablets or capsules wherein the active ingredient is protected by inclusion in an excipient or by separated granulation of the excipients and mixing granulate with a mixture of the active ingredient and a excipient having low moisture content.
33 Citations
8 Claims
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1. A method for the preparation of a pharmaceutical composition in tablet or capsule form containing the active ingredient bromocriptine base or bromocriptine salified with organic or inorganic acids, which method comprises the following steps:
- (a) dissolving the active ingredient in a solvent or mixture of solvents capable of producing a solution having a concentration of active ingredient greater than about 10%, said solvent being selected from ethyl and isopropyl alcohol, acetone, ethyl acetate, chloroform, methylene chloride, water and carbon tetrachloride;
(b) using the resultant solution to wet an excipient, or mixture of excipients, insoluble in said solution but subject to the swelling action thereof, said excipient being selected from cross-linked polyvinylpyrrolidone, cross-linked sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, alginic acid and salts thereof, starch and derivatives thereof and ion exchange resins, whereby an expanded excipient is obtained;
(c) drying said expanded excipient to produce an active ingredient-bearing excipient product having a residual moisture content of less than 1% and subjecting said product to separation; and
(d) compressing said product into tablets or distributing it into capsules. - View Dependent Claims (2, 8)
- (a) dissolving the active ingredient in a solvent or mixture of solvents capable of producing a solution having a concentration of active ingredient greater than about 10%, said solvent being selected from ethyl and isopropyl alcohol, acetone, ethyl acetate, chloroform, methylene chloride, water and carbon tetrachloride;
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3. A method for the preparation of a pharmaceutical composition in tablet or capsule form containing the active ingredient bromocriptine base or bromocriptine salified with organic or inorganic acids, which method comprises the following steps:
- (a) preparing a mixture of the entire amount of active ingredient to be used in said composition with a portion of the total amount of a lactose to be used in said composition, said lactose being of very low residual moisture content;
(b) preparing a granulate of the remaining lactose and an excipient, or mixture thereof, selected from cross-linked polyvinylpyrrolidone, cross-linked sodium carboxymethyl cellulose, calcium carboxymethyl cellulose, alginic acid and salts thereof, starch and derivatives thereof and ion exchange resins, with a solvent, or mixture of solvents, selected from ethyl and isopropyl alcohol, acetone, ethyl acetate, chloroform, methylene chloride, water and carbon tetrachloride;
(c) drying said granulate to a residual moisture content of less than 1% and subjecting said granulate to separation;
(d) forming a mixture of the product of step (a) and the granulate of step (c); and
(e) compressing the mixture of step (d) into tablets or distributing it into capsules. - View Dependent Claims (4, 5, 6, 7)
- (a) preparing a mixture of the entire amount of active ingredient to be used in said composition with a portion of the total amount of a lactose to be used in said composition, said lactose being of very low residual moisture content;
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Current AssigneePolichem, SA (Grupo Corporativo Landon SL)
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Original AssigneePoli Industria Chimica S. P. A.
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InventorsMoro, Luigi, Fiori, Achille, Natali, Alberto
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Primary Examiner(s)Page, Thurman K.
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Assistant Examiner(s)Spear, James M.
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Application NumberUS07/502,520Time in Patent Office599 DaysField of Search424/451, 424/452, 424/457, 424/464, 424/465, 424/8 D, 424/79, 424/489US Class Current424/451CPC Class CodesA61K 31/48 Ergoline derivatives, e.g. ...A61K 9/2077 Tablets comprising drug-con...
