Vaccine formulations comprising saponin-containing adjuvants
The present invention provides for a novel oil-in-water (O/W) emulsion, with increased stability in the presence of bacterial or viral suspensions, especially those concentrated and non-purified (crude extracts) or minimally purified. The emulsion of the present invention can act as vehicle for the delivery of a pharmaceutical composition comprising at least one immunogen and, in particular, an immunogen selected from the group consisting of an inactivated pathogen, an attenuated pathogen, a subunit, a recombinant expression vector, and a plasmid or combinations thereof.
1. A safe and effective stable immunological injectable oil-in-water (O/W) emulsion, wherein the emulsion is effective for eliciting an immunologic response in a vaccinate, comprising:
(i) an aqueous solution comprising about 60 μg of whole inactivated porcine circovirus 2 (PCV2) virus per dose;
(ii) an aqueous solution comprising a saponin in the amount of about 0.7 mg/dose to about 1.3 mg/dose; wherein the saponin consists of an anion-exchange column purified extract of Quillaja saponaria Molina bark enriched for QS-17, QS-18 and QS-21;
(iii) an aqueous solution comprising aluminum hydroxide in the amount of about 0.37% w/v to about 0.42% w/v of the emulsion;
(iv) paraffin oil present in the amount of about 20% to about 40% of the emulsion;
(v) a non-ionic lipophilic surfactant, present in the amount of 0.1% to about 2.5% w/v of the emulsion, and selected from sorbitan fatty acid monoesters, fatty acid esters of mannide, ethoxylated fatty acid esters of mannide, and combinations thereof;
(vi) a non-ionic hydrophilic surfactant present in the amount of 0.1% to about 1.5% w/v of the emulsion, and having a high hydrophilic-lipophilic balance (HLB) value between 13 and 40 selected from ethoxylated fatty acid monoesters of sorbitan, ethoxylated fatty acids, and combinations thereof; and
(vii) a non-ionic hydrophilic surfactant present in the amount of about 1% to about 8% w/v of the emulsion, and having a low hydrophilic-lipophilic balance (HLB) value between 9 and 13 selected from ethoxylated fatty acid triesters of sorbitan, ethoxylated fatty acid diesters of sorbitan, ethoxylated fatty acid monoesters of sorbitan, ethoxylated fatty acids, ethoxylated castor oil and, combinations thereof; and
wherein the final HLB of the emulsion is from about 9 to about 12; and
wherein the emulsion remains an O/W emulsion for at least 24 months; and
wherein the emulsion does not contain any metabolisable oil.
2. The emulsion of claim 1 , wherein the high HLB non-ionic hydrophilic surfactant is present at a concentration of 0.4% to 1.2% expressed as a weight by volume of emulsion (w/v), and wherein the percentage of the surfactants is from about 4% to about 8% weight/volume.
3. The emulsion of claim 1 , wherein the low HLB non-ionic hydrophilic surfactant is present at a concentration of 2.5% to 4% expressed as a weight by volume of emulsion (w/v).
4. The emulsion of claim 1 , wherein the non-ionic lipophilic surfactant is present at a concentration of 0.2% to 1.2% expressed as a weight by volume of emulsion (w/v).
5. The emulsion of claim 1 , wherein the emulsion has a phase inversion temperature (PIT) of between about 36° C. to about 46° C.
6. The emulsion of claim 1 , wherein the low HLB non-ionic hydrophilic surfactant is an ethoxylated fatty acid triester of sorbitan, and wherein the ester of said ethoxylated fatty acid ester is selected from the group consisting of oleate, palmitate, stearate, isostearate, laurate and combinations thereof.
7. The emulsion of claim 1 , wherein the non-ionic lipophilic surfactant is a fatty acid ester of sorbitan, and wherein the ester of the fatty acid ester is selected from the group consisting of oleate, palmitate, stearate, isostearate, laurate and combinations thereof.
8. The emulsion of claim 1 , wherein the high HLB non-ionic hydrophilic surfactant is an ethoxylated fatty acid monoester of sorbitan, and wherein the ethoxylated monoester of sorbitan is selected from the group consisting of ethoxylated sorbitan monolaurate, ethoxylated sorbitan monopalmitate, ethoxylated sorbitan monostearate, ethoxylated sorbitan monooleate, and combinations thereof.
9. The emulsion of claim 1 , wherein the mineral oil is selected from the group consisting of paraffin oil, squalane, pristane, polyisobutene oil, hydrogenated polyisobutene oil, polydecene oil, polyisoprene oil, polyisopropene oil, and combinations thereof.
10. A method for inducing an immunological response in an animal against a pathogen comprising administering to said animal the emulsion of claim 1 .
11. The emulsion of claim 1 , wherein the amount of saponin is about 0.7 mg/dose.