Method for preparing small vesicles using microemulsification

Claim 2

A process for the preparation of small, unilamellar vesicles of less than 2000 Å suitable for biological applications comprising: (a) hydrating amphilillic molecules selected from the group consisting of phospholipids and phosphoglycerides having hydrocarbon chains of at least 16 carbon atoms, and other components capable of forming lipid vesicles that are stable in vivo; (b) dispersing said hydrated lipid in a homogenizing apparatus at a pressure within the range of approximately 8000 to approximately 13,000 psi and at a selected temperature maintained in the range of approximately 50° C. to 80° C. for time periods ranging from 15 to 90 minutes to generate a microemulsion containing small unilamellar lipid vesicles of less than 2000 Å; and (c) separating said small, unilamellar vesicles from unencapsulated materials.

Claim 3

The process according to claim 1 wherein said amphiphilic molecules are phospholipids selected from the group consisting of phosphatidylcholine, phosphatidylethanolamine and phosphatidylserine.

Claim 4

The process according to claim 1 wherein the amphiphilic molecules are selected from the group consisting of distearoyl phosphatidylcholine and dipalmitoyl phosphatidylcholine.

Claim 5

The process as defined in claim 1 wherein said step of dispersing is performed by operating said homogenizing apparatus at pressures in the range of approximately 8000 to 10,000 psi and at a reservoir temperature in the range of approximately 70°-75° C. for 60 minutes.

Claim 6

The process as defined in claim 1 wherein said step of dispersing is performed by operating the homogenizing apparatus at pressures in the range of approximately 10,000 to 12,000 psi and at a reservoir temperature in the range of approximately 50°-55° C. for 60 minutes.

Claim 7

The process according to claim 1 wherein said step of hydrating amphiphilic molecules capable of forming lipid vesicles includes the steps of: (a) dissolving said amphiphilic molecules and other components capable of forming lipid vesicles in an organic solvent solution; (b) drying said solution to a lipid film; and (c) rehydrating the dried lipid film.

Claim 8

The process as defined by claim 6 wherein said organic solvent is selected from the group consisting of ethers, chloroform and alcohol.

Claim 9

The process according to claim 1 wherein the amphiphilic molecules and other components capable of forming lipid vesicles are phospholipid and cholesterol in the mole ratio of 2 to 1.

Claim 10

The process as defined in claim 1 wherein the composition of vesicles comprises phospholipid, cholesterol and a therapeutic agent said therapeutic agent being contained in the solution used to hydrate the amphiphillic molecules.

Claim 11

The process as defined in claim 9 where said therapeutic agent is a chemotherapeutic agent.

Claim 12

The process according to claim 10 wherein said chemotherapeutic agent is selected from the group of antibiotics consisting of Daunomycin, Bleomycin, Adriamycin, Actinomycin D, Mytomycin C and Mithramycin.

Claim 13

The process according to claim 10 wherein said chemoratherapeutic agent is selected from the group of alkylating agents consisting of chlorambucil, cyclophosphamide and Triethylenemelamine.

Claim 14

The process according to claim 10 wherein said chemotherapeutic agent is selected from the group of antimetabolites consisting of methotrexate, 5-Fluorouracil, 6-Mercaptopurine and Arabinosylcytosine.

Claim 15

The process according to claim 9 whereinsaid therapeutic agent is a radiotherapeutic agent.

Claim 16

The process according to claim 14 wherein said radiotherapeutic agent is selected from the group consisting of the radionuclides Iodine 131, Yttrium 90 and Phosphorus 32.

Claim 17

A process for the preparation of small unilamellar vesicles of less than 2000 Å suitable for use in targeting tumors in a body for location and diagnosis of the tumors comprising the steps of: (a) dissolving amphiphilic molecules selected from the group consisting of phospholipids and phosphoglycerides having hydrocarbon chains of at least 16 carbon atoms, and other components capable of forming lipid vesicles that are stable in vivo in an organic solvent solution; (b) drying said solution to a lipid film; (c) rehydrating the dried lipid film with phosphate buffered saline containing a weak chelating agent; (d) dispersing said rehydrated lipid in a homogenizing apparatus at a pressure within the range of approximately 8000 to approximately 13,000 psi and at a selected temperature maintained in the range of approximately 50° to 80° C. for time periods ranging from 15 to 90 minutes to generate a microemulsion containing small unilamellar lipid vesicles of less than 2000 Åwith an ionophore incorporated into the lipid bilayer and said vesicles containing the chelating agent; (e) separating said small unilamellar vesicles from unencapsulated vesicle precursor materials; and (f) loading said vesicles with radioactive cation for detecting the location of said vesicles when administered into a body.

Claim 18

A process for the preparation of small unilamellar vesicles of less than 2000 Å suitable for use in targeting tumors in a body for location and diagnosis of the tumors comprising the steps of: (a) dissolving amphiphilic molecules selected from the group consisting of phospholipids and phosphoglycerides having hydrocarbon chains of at least 16 carbon atoms, and other components capable of forming lipid vesicles that are stable in vivo in an organic solvent solution; (b) drying said solution to a lipid film; (c) rehydrating the dried lipid film with phosphate buffered saline containing a weak chelating agent; (d) dispersing said rehydrated lipid in a homogenizing apparatus at a pressure within the range of approximately 8000 to approximately 13,000 psi and at a selected temperature maintained in the range of approximately 50° to 80° C. for time periods ranging from 15 to 90 minutes to generate a microemulsion containing small unilamellar lipid vesicles of less than 2000 Åwith an ionophore incorporated into the lipid bilayer and said vesicles containing the chelating agent; (e) separating said small unilamellar vesicles from unencapsulated vesicle precursor materials; and (f) loading said vesicles with radioactive cation for detecting the location of said vesicles when administered into a body.

Claim 19

The process according to claim 16 wherein said amphiphilic molecules are phospholipids and said other components capable of forming vesicles are cholesterol and an ionophore.

Claim 20

The process as defined in claim 17 wherein the phospholipid is selected from a group consisting of distearoyl phosphatidylcholine and dipalmitoyl phosphatidylcholine.

Claim 21

The process according to claim 17 wherein the ionophore is A23187.

Claim 22

The process according to claim 17 wherein the composition of the vesicles comprises phospholipid, cholesterol and ionophore in the mole ratio 2:1:0.004.

Claim 23

The process as defined in claim 16 wherein the chelating agent is nitriloacetic acid.

Claim 24

The process according to claim 16 wherein the radioactive cation is 111 In +3 .