An improved method for the manufacture of an oil-in-water emulsion involves three procedures: (i) preparation of a preliminary emulsion; (ii) microfluidization of the preliminary emulsion to reduce its droplet size; and (iii) filtration of the microfluidized emulsion through a hydrophilic membrane.

Patent
   RE46906
Priority
Dec 03 2009
Filed
Oct 13 2015
Issued
Jun 26 2018
Expiry
Dec 03 2030

TERM.DISCL.
Assg.orig
Entity
Large
2
73
currently ok
1. A method for the manufacture of a squalene-containing oil-in-water emulsion vaccine adjuvant, the method comprising the step of: (i) formation of a first emulsion having a first average oil droplet size using a mechanical homogenizer, wherein the first emulsion is formed by a type ii circulation of transferring its the first emulsion components from a first container to a second container through a homogenizer, and then returning them from the second container to the first container through the same homogenizer, wherein substantially all of the emulsion components from the first container are passed through the homogenizer into the second container, and then substantially all of the emulsion components from the second container are passed through the homogenizer back into the first container; and (ii) microfluidizing the first emulsion to form a second emulsion having a second average oil droplet size which is less than the first average oil droplet size.
2. The method of claim 1, wherein step (i) comprises two or more cycles of transferring the first emulsion's components from the first container to the second container and back again.
3. The method of claim 1, wherein the homogenizer is a rotor-stator homogenizer and wherein the microfluidization occurs in an interaction chamber having no moving parts.
4. The method of claim 1, wherein the homogenizer provides a shear rate of up to 1×106 s−1, and wherein the microfluidization occurs an interaction chamber that provides a shear rate >2.5×106 s−1.
5. The method of claim 1, comprising: (iii) filtration of the second emulsion.
6. The method of claim 1, wherein during step (ii), the second emulsion is formed by circulating the second emulsion components through a microfluidization device a plurality of times.
7. The method of claim 6, wherein the circulation of the second emulsion components comprises transferring the second emulsion components between a first emulsion container and a microfluidization device; and (iii) microfluidizing the first emulsion to form a second emulsion having a second average oil droplet size which is less than the first average oil droplet size.
8. The method of claim 6, wherein the circulation of the second emulsion components comprises transferring the second emulsion components from a first emulsion container, through a microfluidization device to a second emulsion container, and then again through the microfluidization device.
9. The method of claim 1, wherein the first average oil droplet size is 5000 nm or less.
10. The method according to claim 1, wherein the number of oil droplets having a size of >1.2 μm in the first emulsion is 5×1011/ml or less.
11. The method of claim 1, wherein the second average oil droplet size is 500 nm or less.
12. The method of claim 1, further comprising combining the emulsion with an antigen to produce a vaccine composition.
13. The method of claim 1, further comprising packaging the emulsion into a kit as a kit component together with an antigen component.
14. The method of claim 1, wherein the components of the first emulsion are combined in a mixing vessel before being introduced into the homogenizer.
15. The method of claim 14, wherein the homogenizer is a rotor-stator homogenizer.
16. The method of claim 1, wherein the first and second containers are held under an inert gas.
17. The method of claim 6, wherein the second emulsion is formed by circulating the second emulsion components through a microfluidization device three times.
18. The method of claim 1, wherein the first and second emulsion containers are held under an inert gas.
0. 19. The method of claim 1, wherein the first emulsion is formed by circulation comprising (a) a type I circulation of transferring the first emulsion components between a first container and a homogenizer followed by (b) the type ii circulation.

This application a type I (FIG. 5) followed by a type II (FIG. 6) circulation. For five separate runs the average number of larges larger particles per ml was as follows:

Mean Coefficient of variation
Type I 1.70 × 109 0.23
Type I followed by Type II 1.04 × 109 0.13

Thus the inclusion of type II circulation results in fewer large droplets and less batch-to-batch variation.

It will be understood that the invention has been described by way of example only and modifications may be made whilst remaining within the scope and spirit of the invention.

References

Rueckl, Harald, Scheffczik, Hanno, Santry, Barbara

Patent Priority Assignee Title
10463615, Dec 03 2009 Novartis AG Circulation of components during microfluidization and/or homogenization of emulsions
11141376, Dec 03 2009 Novartis AG Circulation of components during microfluidization and/or homogenization of emulsions
Patent Priority Assignee Title
4533254, Apr 17 1981 PNC BANK, NATIONAL ASSOCIATON Apparatus for forming emulsions
5487965, Sep 06 1994 Xerox Corporation Processes for the preparation of developer compositions
5510118, Feb 14 1995 Alkermes Pharma Ireland Limited Process for preparing therapeutic compositions containing nanoparticles
5565203, May 08 1991 Crucell Switzerland AG Hepatitis A virus in a reconstituted influenza virosome and use as a vaccine
6168718, Nov 08 1996 HAEMONETICS PUERTO RICO, LLC Method for purifying blood plasma and apparatus suitable therefor
6331314, Nov 15 1995 Bayer Intellectual Property GmbH Method and device for producing a parenteral medicament
6364919, Aug 20 1999 Cheil Industries, Inc. Process for preparing metal oxide slurries suitable for the chemical mechanical polishing of semiconductors
6645463, May 16 1994 MICHIGAN, UNIVERSITY OF, BOARD OF REGENTS OF THE Blood-pool selective carrier for lipophilic imaging agents
7122191, Apr 05 2004 Zoetis Services LLC Microfluidized oil-in-water emulsions and vaccine compositions
7238349, Sep 30 1999 SMITHKLINE BEECHAM BIOLOGICALS S A ; SAECHSISCHES SERUMWERK DRESDEN BRANCH OF SMITHKLINE BEECHAM PHARMA GMBH Composition
8182792, Mar 23 2004 Novartis AG Pharmaceutical compositions
8187554, Apr 23 2008 MICROFLUIDICS INTERNATIONAL CORPORATION Apparatus and methods for nanoparticle generation and process intensification of transport and reaction systems
8506966, Feb 22 2008 Seqirus UK Limited Adjuvanted influenza vaccines for pediatric use
8678184, Dec 03 2009 Novartis AG Methods for producing vaccine adjuvants
8771727, Apr 04 2003 Zoetis Services LLC Microfluidized oil-in-water emulsions and vaccine compositions
8778275, Dec 03 2009 Novartis AG Methods for producing vaccine adjuvants
8871816, Dec 03 2009 Novartis AG Methods for producing vaccine adjuvants
8895629, Dec 03 2009 Novartis AG Circulation of components during homogenization of emulsions
20020048606,
20020071870,
20040029977,
20040258701,
20060144973,
20060148776,
20060251684,
20060280643,
20070172426,
20070248632,
20080026981,
20080069832,
20090258043,
20090263422,
20100173854,
20110162982,
20110165193,
20120315308,
20130129786,
20150017206,
20160113870,
CN1767854,
CN1956729,
CN1972670,
DE10059430,
DE19542499,
EP770422,
EP1020760,
EP1574210,
GB10096717,
TW200611880,
WO2009123595,
WO2011067669,
WO243672,
WO487204,
WO9155401,
WO199405298,
WO2000050006,
WO2004082625,
WO2004087204,
WO2005027872,
WO2005089718,
WO2006008504,
WO2006050837,
WO2006100110,
WO2006100111,
WO2007098186,
WO2008051186,
WO2008068631,
WO2009132171,
WO2009155401,
WO2011067672,
WO2011067673,
WO2011154442,
WO9014837,
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Jan 07 2013SANTRY, BARBARANovartis Vaccines and Diagnostics GmbHASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0412250783 pdf
Jan 22 2013SCHEFFCZIK, HANNONovartis Vaccines and Diagnostics GmbHASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0412250783 pdf
Feb 20 2013Novartis Vaccines and Diagnostics GmbHNovartis AGASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0412260093 pdf
Oct 13 2015Novartis AG(assignment on the face of the patent)
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