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US3063905A Expired / Lapsed US ⏱️ 0.0 years remaining

Carboxy methyl benzyl dextran dextro-amphetamine

Assignee: Central Pharmacal Co
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Filing: 1959-08-21
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Granted: 1962-11-13
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Expires: 1979-08-21
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Abstract

Abstract A sustained release pharmaceutical product comprises a medicinally-active substance in combination with a carboxy alkyl benzyl dextran. The dextran derivative is preferably a carboxymethyl benzyl dextran having a high benzyl degree of substitution (D.S) and a relatively low carboxyl D.S. obtained by treating dextran in water at 40 DEG C. with sodium monochloroacetate and subsequently with benzyl chloride using a ratio of 3:1 to 6:1 of the chloride to the substituted dextran. It may be used in a proportion between 1 and 50% by weight of the pharmaceutical product. Medicaments which may be combined with the substituted dextran are amphetamine hydrochloride, penicillin, streptomycin, chloroprophenyridamine, meperidine, codeine, ephedrine, quinine, quinidine, nicotine, cinchonidine, apmorphine, strychnine, scopolamine or atropine. Inert fillers such as terra alba and starch; and antihistamines, barbiturates, glycols, soya bean oil, sesame oil, hydrogenated peanut oil and a mixture of oils with beeswax may also be added. The pharmaceutical product may be used as a dry powder or mixed with liquids to form pastes or wax-like masses, compressed into tablets, pills or pellets or packaged into dry-filled or soft elastic capsules, or sealed into ampoules, or administered in liquid form by intravenous, intramuscular, sublingual, subcutaneous, rectal, intraspinous or intrathecal injection or infused into the vaginal or urinary tract.ALSO:A sustained release pharmaceutical product comprises a medicinally-active substance in combination with a carboxy alkyl benzyl dextran. The dextran derivative is preferably a carboxymethyl benzyl dextran having a high benzyl degree of substitution (D.S.) and a relatively low carboxyl D.S. obtained by treating dextran in water at 40 DEG C. with sodium monochloroacetate and subsequently with benzyl chloride using a ratio of 3:1 to 6:1 of the chloride to the substituted dextran. It may be used in a proportion between 1 and 50% by weight of the pharmaceutical product. Medicaments which may be combined with the substituted dextran include penicillin and streptomycin, which form salts with the dextran derivative.ALSO:A sustained release pharmaceutical product comprises a medicinally-active substance in combination with a carboxy alkyl benzyl dextran. The destran derivative is preferably a carboxymethyl benzyl dextran having a high benzyl degree of substitution (D.S.) and a relatively low carboxyl D.S. obtained by treating dextran in water at 40 DEG C. with sodium monochloroacetate and subsequently with benzyl chloride using a ratio of 3 : 1 to 6 : 1 of the chloride to the substituted dextran. It may be used in a proportion between 1 and 50% by weight of the pharmaceutical product. Medicaments which may be combined with the substituted dextran are amphetamine hydrochloride penicillin, streptomycin, chloroprophenyridamine, meperidine, codeine, ephedrine, quinine, quinidine, nicotine, cinchonidine, apomorphine, strychnine, scopolamine or atropine. Inert fillers such as terra alba and starch; and antihistamines, barbiturates, glycols, soya bean oil, sesame oil, hydrogenated peanut oil and a mixture of oils with beeswax may also be added. The pharmaceutical product may be used as a dry powder or mixed with liquids to form pastes or wax-like masses, compressed into tablets, pills or pellets or packaged into dry-filled or soft elastic capsules, or sealed into ampoules, or administered in liquid form by intravenous, intramuscular, sublingual, subcutaneous, rectal, intraspinous or intrathecal injection or infused into the vaginal or urinary tract.

Inventors

  • 👤 Leo J Novak

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 12:20
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/70; A61K31/33; A61K31/395; A61K31/41; A61K31/425; A61K31/429; A61K31/43; A61K47/00; A61K47/30; A61K47/36; A61K47/50; A61K47/51; A61K47/56; A61K47/58; A61K47/585; C; C08; C08B; C08B37/00; C08B37/0006; C08B37/0009; C08B37/0021

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 70 words
A SUSTAINED RELEASE PHARMACEUTICAL PRODUCT FOR INTRODUCING INTO THE INTESTINAL TRACT COMPRISING A DEXTROAMPHETAMINE DRUG COMBINED WITH CARBOXY METHYL BENZYL DEXTRAN WHICH IS RESISTANT TO DISINTEGRATION AND SLOWLY RELEASES THE DRUG IN THE GASTRO-INTESTINAL TRACT, SAID CARBOXY METHYL BENZYL DEXTRAN COMPRISING 1 TO 50% BY WEIGHT OF SAID PHARMACEUTICAL PRODUCT, SAID CARBOXYMETHYL BENZYL DEXTRAN HAVING THE D.S. OF CARBOXYMETHYL HELD TO 1.5 AND THE D.S. OF BENZYLE HELD TO 1.5.
Claim 2
Dependent Claim 70 words
A SUSTAINED RELEASE PHARMACEUTICAL PRODUCT FOR INTRODUCING INTO THE INTESTINAL TRACT COMPRISING A DEXTROAMPHETAMINE DRUG COMBINED WITH CARBOXY METHYL BENZYL DEXTRAN WHICH IS RESISTANT TO DISINTEGRATION AND SLOWLY RELEASES THE DRUG IN THE GASTRO-INTESTINAL TRACT, SAID CARBOXY METHYL BENZYL DEXTRAN COMPRISING 1 TO 50% BY WEIGHT OF SAID PHARMACEUTICAL PRODUCT, SAID CARBOXYMETHYL BENZYL DEXTRAN HAVING THE D.S. OF CARBOXYMETHYL HELD TO 1.5 AND THE D.S. OF BENZYLE HELD TO 1.5.

References Cited (Backward Citations)

US2536168A Cited
US2609368A Cited
US2749274A Cited
US2811516A Cited
US2885393A Cited
US2856398A Cited
US2902408A Cited
US2997423A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1965-11-12 1966-05-14 1966-11-13 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1969-11-12 1970-05-14 1970-11-13 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1973-11-12 1974-05-14 1974-11-13 $7700.00 Window Closed / Lapsed

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