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US4518547A Expired / Lapsed US ⏱️ 0.0 years remaining

Microencapsulation process

Assignee: The University of Texas System
•
Filing: 1983-09-15
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Granted: 1985-05-21
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Expires: 2003-09-15
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Abstract

Abstract Nylon coated microcapsules containing hydrophilic solvent-soluble anionic, cationic or quaternary drug salts were prepared by interfacial polycondensation techniques. In a first stage, the drug substance to be encapsulated is dissolved in an aqueous phase. Examples of drugs encapsulated are morphine sulfate, diphenhydramine hydrochloride, and methantheline bromide. Next the aqueous drug solution is dispersed in an organic phase. In a second stage complementary polycondensation reactants each in an organic phase are added separately, either sequentially or simultaneously, to the dispersion prepared in the first stage. Microcapsules of nylon form around the hydrophilic solvent soluble core drug substance.

Inventors

  • 👤 George W. Cuff
  • 👤 James W. McGinity

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 08:37
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/48; A61K9/50; B; B01; B01J; B01J13/00; B01J13/02; B01J13/06; B01J13/14; B01J13/16

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 133 words
A process for the encapsulation of a hydrophilic core material in a membrane formed by interfacial polycondensation, the process comprising: in a first step, dispersing in a first continuous hydrophobic phase a hydrophilic phase comprising in solution the hydrophilic material to be encapsulated and a hydrophilic solvent or water; and then in a second stage, adding separately to the dispersion either sequentially or simultaneously, each of two complementary polycondensation monomer reactants: the first polycondensation monomer reactant comprising a hydrophobic solvent-soluble reagent; the second polycondensation monomer reactant comprising a hydrophilic solvent-soluble reagent dispersed in a second continuous hydrophobic phase; allowing the polycondensation monomers to react, the reaction effective to cause interfacial polymerization of a membrane encapsulating the hydrophilic phase containing the hydrophilic core material; and separating the encapsulated material from the continuous hydrophobic phase.
Claim 2
Dependent Claim 133 words
A process for the encapsulation of a hydrophilic core material in a membrane formed by interfacial polycondensation, the process comprising: in a first step, dispersing in a first continuous hydrophobic phase a hydrophilic phase comprising in solution the hydrophilic material to be encapsulated and a hydrophilic solvent or water; and then in a second stage, adding separately to the dispersion either sequentially or simultaneously, each of two complementary polycondensation monomer reactants: the first polycondensation monomer reactant comprising a hydrophobic solvent-soluble reagent; the second polycondensation monomer reactant comprising a hydrophilic solvent-soluble reagent dispersed in a second continuous hydrophobic phase; allowing the polycondensation monomers to react, the reaction effective to cause interfacial polymerization of a membrane encapsulating the hydrophilic phase containing the hydrophilic core material; and separating the encapsulated material from the continuous hydrophobic phase.
Claim 3
Dependent Claim 22 words
The process according to claim 1 wherein the hydrophilic core comprises water soluble salts of anionic, cationic, quaternary, amphoteric or nonionic compounds.
Claim 4
Dependent Claim 21 words
The process according to claim 1 wherein the first or second continuous hydrophobic phase is a solution of cyclohexane and chloroform.
Claim 5
Dependent Claim 29 words
The process according to claim 1 wherein the first polycondensation monomer is selected from the group consisting of multifunctional acid halides, diacids, diisocyanates, multifunctional sulfonyl halides, and mixtures thereof.
Claim 6
Dependent Claim 16 words
The process according to claim 1 wherein the first polycondensation monomer is a multifunctional acid halide.
Claim 7
Dependent Claim 14 words
The process according to claim 5 wherein the multifunctional acid halide is sebacyl chloride.
Claim 8
Dependent Claim 34 words
The process according to claim 1 wherein the second polycondensation monomer reactant is selected from the group consisting of polyfunctional amines, polyols, diamines, and diols, and mixtures thereof dispersed in a hydrophobic continuous phase.
Claim 9
Dependent Claim 15 words
The process according to claim 1 wherein the second polycondensation monomer reactant is a diamine.
Claim 10
Dependent Claim 11 words
The process according to claim 8 wherein the diamine is hexamethylenediamine.
Claim 11
Dependent Claim 22 words
The process according to claim 1 wherein both the first and second polycondensation monomer reactants are added simultaneously to the first dispersion.

References Cited (Backward Citations)

US3575882A Cited
US3886084A Cited
US4324683A Cited
US4251386A Cited
US4219604A Cited
US4309213A Cited
US4322311A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-05-20 1988-11-19 1989-05-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-05-20 1992-11-19 1993-05-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-05-20 1996-11-19 1997-05-21 $7700.00 Window Closed / Lapsed

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