EP2217362A2 - Microparticules encapsulées présentant un noyau qui contient des virus, et procédé de préparation des microparticules - Google Patents
Microparticules encapsulées présentant un noyau qui contient des virus, et procédé de préparation des microparticulesInfo
- Publication number
- EP2217362A2 EP2217362A2 EP08854538A EP08854538A EP2217362A2 EP 2217362 A2 EP2217362 A2 EP 2217362A2 EP 08854538 A EP08854538 A EP 08854538A EP 08854538 A EP08854538 A EP 08854538A EP 2217362 A2 EP2217362 A2 EP 2217362A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- microparticles
- microparticle
- viruses
- range
- bar
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000011859 microparticle Substances 0.000 title claims abstract description 42
- 241000700605 Viruses Species 0.000 title claims abstract description 40
- 238000004519 manufacturing process Methods 0.000 title description 6
- 150000003626 triacylglycerols Chemical class 0.000 claims abstract description 19
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 8
- 229930195729 fatty acid Natural products 0.000 claims abstract description 8
- 239000000194 fatty acid Substances 0.000 claims abstract description 8
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 22
- PVNIQBQSYATKKL-UHFFFAOYSA-N tripalmitin Chemical group CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC PVNIQBQSYATKKL-UHFFFAOYSA-N 0.000 claims description 20
- 241000537222 Betabaculovirus Species 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 16
- 239000002775 capsule Substances 0.000 claims description 14
- 239000001569 carbon dioxide Substances 0.000 claims description 14
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 14
- 239000007789 gas Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 239000000654 additive Substances 0.000 claims description 12
- 239000000155 melt Substances 0.000 claims description 12
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000012963 UV stabilizer Substances 0.000 claims description 10
- 229960001947 tripalmitin Drugs 0.000 claims description 10
- 241000701447 unidentified baculovirus Species 0.000 claims description 10
- 241001074088 Urophycis Species 0.000 claims description 8
- 239000003995 emulsifying agent Substances 0.000 claims description 8
- 238000009835 boiling Methods 0.000 claims description 7
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 239000003016 pheromone Substances 0.000 claims description 7
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 6
- 238000000517 particles from gas-saturated solution Methods 0.000 claims description 6
- 235000000346 sugar Nutrition 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 5
- 239000001294 propane Substances 0.000 claims description 5
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 239000001272 nitrous oxide Substances 0.000 claims description 3
- 235000020183 skimmed milk Nutrition 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims description 2
- CGZKSPLDUIRCIO-UHFFFAOYSA-N Scytonemin Natural products OC1=CC=C(C=C1)C=C1C(C(=C2C1=NC=1C=CC=CC2=1)C=1C(C(C2=NC=3C=CC=CC=3C2=1)=CC1=CC=C(C=C1)O)=O)=O CGZKSPLDUIRCIO-UHFFFAOYSA-N 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 239000001273 butane Substances 0.000 claims description 2
- 235000021466 carotenoid Nutrition 0.000 claims description 2
- 150000001747 carotenoids Chemical class 0.000 claims description 2
- OPCRGEVPIBLWAY-HWDIUJSMSA-N ethyl (2Z)-deca-2,4-dienoate Chemical compound C(C)OC(\C=C/C=CCCCCC)=O OPCRGEVPIBLWAY-HWDIUJSMSA-N 0.000 claims description 2
- 229930003935 flavonoid Natural products 0.000 claims description 2
- 150000002215 flavonoids Chemical class 0.000 claims description 2
- 235000017173 flavonoids Nutrition 0.000 claims description 2
- 229930195712 glutamate Natural products 0.000 claims description 2
- 239000000787 lecithin Substances 0.000 claims description 2
- 235000010445 lecithin Nutrition 0.000 claims description 2
- 229940067606 lecithin Drugs 0.000 claims description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 2
- 239000001814 pectin Substances 0.000 claims description 2
- 235000010987 pectin Nutrition 0.000 claims description 2
- 229920001277 pectin Polymers 0.000 claims description 2
- CGZKSPLDUIRCIO-RPCRKUJJSA-N scytonemin Chemical compound C1=CC(O)=CC=C1\C=C\1C2=NC3=CC=CC=C3C2=C(C=2C(C(=C/C=3C=CC(O)=CC=3)/C=3C=2C2=CC=CC=C2N=3)=O)C/1=O CGZKSPLDUIRCIO-RPCRKUJJSA-N 0.000 claims description 2
- 241001635274 Cydia pomonella Species 0.000 description 9
- 241000220225 Malus Species 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000003925 fat Substances 0.000 description 5
- 241000607479 Yersinia pestis Species 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000003612 virological effect Effects 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 239000005667 attractant Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 241001135545 Cydia pomonella granulovirus Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000255967 Helicoverpa zea Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- UPYKUZBSLRQECL-UKMVMLAPSA-N Lycopene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1C(=C)CCCC1(C)C)C=CC=C(/C)C=CC2C(=C)CCCC2(C)C UPYKUZBSLRQECL-UKMVMLAPSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000003124 biologic agent Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001746 carotenes Chemical class 0.000 description 1
- 235000005473 carotenes Nutrition 0.000 description 1
- 230000031902 chemoattractant activity Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011217 control strategy Methods 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 210000002490 intestinal epithelial cell Anatomy 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 230000007918 pathogenicity Effects 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/04—Making microcapsules or microballoons by physical processes, e.g. drying, spraying
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/40—Viruses, e.g. bacteriophages
Definitions
- the invention relates to encapsulated microparticles having a core containing viruses in free or carrier-bound form and a shell enclosing the core.
- the invention further relates to an associated manufacturing method for the microparticles.
- the encapsulation serves in particular to improve the UV stability and increase the rate of uptake of baculoviruses by a host organism used for pest control.
- viruses for pest control is sought in organic and integrated agriculture.
- the commercial use of viral particles necessitates the finding of formulations which permit a practicable handling of the viruses, that is to say the particular preparations to be used must have sufficient stability in the field of use, a sufficient dosage of viral particles and, if appropriate, satisfy existing safety regulations.
- baculovirus-based biological insecticides combine positive ecological and economic aspects.
- Baculoviruses against cotton bollworm, sponge moth, codling moth and apple peel winder In Germany, only baculoviruses of the genus granulovirus currently have a license. These are the apple peel worm granulovirus and codling granulovirus.
- Granuloviruses generally have the property that they attack only the larval stages of their host (insects). In order to develop their pathogenicity, they must be actively taken up by the host and then endocytosed into the intestinal epithelial cells in the digestive tract, where they pass into their virulent form. As a result, the infected larvae are killed within 5 to 9 days and cause no damage to the apple. In practice, however, it has been found that the uptake rate of the virus is too low, with the consequence that the codling moth does not die shortly after eating and / or boring into the apple.
- Arthurs et al. describe first the preparation and use of spray-dried, lignin-encapsulated formulations of the granulovirus CpGV for controlling Cydia pomonella, wherein the formulation TiC> 2 is used as UV stabilizer and sugar as Frausslockstoff (Evaluation of spray-dried lignin-based formulations and adjuvant as solar protectants for the granulovirus of the codling moth, Cydia pomonella (L) - Arthurs, SP; Lacey, LA; Behle, RW; Yakima Agricultural Research Laboratory, USA; Journal of Invertebrate Pathology (2006), 93 (2), 88-95 ).
- the invention is based on encapsulated microparticles having a core which contains viruses in free or carrier-bound form and a shell which encloses the core.
- the microparticles according to the invention are characterized in that the shell to at least 50% by weight of one or more triacylglycerides having a chain length of the fatty acids of C10 to C24.
- the invention is based on the finding that saturated or unsaturated triacylglycerides having a chain length of the fatty acids with a length of 10 to 24 carbon atoms allow the encapsulation of viruses in free or carrier-bound form without their viral activity being inhibited.
- the choice of material for the shell has, inter alia, the advantage that they allow rapid resorption of the virus after ingestion by the host, because it is precisely these fats happen easily epithelial cells in the digestive tract of the pests.
- the triacylglyceride shell is particularly suitable for serving as a matrix for further additives, especially if they have a hydrophobic character. Kern within the meaning of the invention is understood to mean all components of the microparticle encompassed by the shell.
- the core need not be compact as a singulated particle, but may contain multiple, separate fragments. It is therefore conceivable to encapsulate several carrier fragments for the viruses with a common shell.
- the shell consists of at least 70% by weight of triacylglycerides.
- Triacylglycerides are esters of the trivalent alcohol glycerol with three fatty acid molecules. Natural fats consist for the most part of triacylglycerides with three long-chain fatty acids, which usually consist of unbranched chains having 4 to 26, typically 12 to 22 carbon atoms. For the purposes of the invention are particularly suitable fatty acids having 10 to 24 carbon atoms.
- the triacylglyceride preferably has a melting point in the range of 10 to 100 0 C, in particular in the range of 25 to 80 0 C, particularly preferably in the range of 25 to 65 ° C.
- the triacylglyceride is tripalmitin or a tripalmitin-containing mixture of triacylglycerides, in particular palm fat.
- Palm fat is characterized on the one hand by its low production costs and on the other contains carotene, which, as will be explained in more detail below, can serve as a UV stabilizer to protect the biological agent.
- tripalmitin or tripalmitin-containing mixtures, such as palm oil are the main ingredients of apple cores and leaf adults and thus act as feed attractants for the codling moth, and are therefore particularly preferred in connection with the use of codling granulovirus.
- the microparticles preferably have an average diameter in the range from 500 nm to 500 ⁇ m, in particular from 1 to 50 ⁇ m. Microparticles of this size can be discharged in particular with the already existing in agriculture conventional spray devices.
- the number of viruses per microparticle should preferably be 1 to 10, more preferably 1 to 2 viruses per particle.
- the shell contains an emulsifier as an additive.
- the emulsifier is a mono- and diacylglyceride, lecithin, pectin, a sugar ester or mixtures thereof.
- a proportion of the emulsifier in the total weight of the microparticle is preferably between 0.1 and 15% by weight.
- the emulsifier serves primarily to facilitate the preparation of an aqueous suspension containing the microparticles.
- a further preferred embodiment which can again be implemented in combination with all of the aforementioned embodiments, provides that the shell contains a UV stabilizer as an additive.
- the UV stabilizer serves to improve the stability of the viruses to natural UV radiation.
- the UV stabilizer used is preferably TiC> 2 , carotenoids, flavonoids, skimmed milk powder, mycosporine-like amino acids (MAA), scytonemin or mixtures thereof.
- the use of UV stabilizers is particularly advantageous in the codling granulovirus.
- the shell may contain a Frriblockstoff as an additive.
- the Frriblockstoff is preferably a pheromone, in particular 2 (E), 4 (Z) - Ethyldecadienoat, glutamate or sugar, in particular sucrose, glucose or fructose.
- Many pheromones are highly volatile, so that their biological effect no longer exists shortly after delivery. However, many of these pheromones are lipophilic, so incorporation into a lipophilic matrix delays the release behavior to the desired extent. This applies in particular to the aforementioned attractant of codling granulovirus.
- the compound mentioned serves as a pheromone for adult females as well as Frriblockstoff for codling larvae.
- baculoviruses in particular from the genus granulovirus.
- the microparticles very particularly advantageously contain apple peel winder granuloviruses or codling granuloviruses.
- a particularly preferred microparticle for the latter two viruses contains as triacylglyceride tripalmitin and / or a tripalmitin-containing mixture, in particular palm fat.
- this microparticle contains 2 (E), 4 (Z) - Ethylenedecadienoate as Frausslockstoff and a UV stabilizer.
- the viruses can be used in ring form or else bound to a carrier. Other, the stabilization of the virus serving additives are possible.
- Another aspect of the invention is to provide a method of making an encapsulated microparticle.
- the method according to the invention comprises the steps:
- PGSS plant Providing a capsule material which consists of at least 50% by weight of one or more triacylglycerides having a chain length of the fatty acids of C10 to C24 in a pressure vessel of a high pressure particulate generation plant (PGSS plant);
- Spraying the melt through a nozzle or capillary Spraying the melt through a nozzle or capillary.
- the so-called PGSS process is a high-pressure method for producing particles.
- any number of liquefiable solids can be mixed and processed into free-flowing powder.
- supercritical fluids are used as auxiliaries. Melting is homogenized and pulverized by mixing the liquefied individual components with compressed carbon dioxide and subsequently depressurizing them, for example via a nozzle. The melt is thereby torn into tiny droplets. It forms the finest powder, which opens up new applications due to its specifically adjustable size (nanometer to micrometer), morphology and composition.
- the PGSS process can be operated both continuously and batchwise.
- the compressed gas is preferably selected from the group consisting of carbon dioxide, nitrous oxide, alkanes having a boiling point of less than 50 0 C at 1 bar, alkenes having a boiling point of less than 50 0 C at 1 bar, hydrofluorocarbons having a boiling point less than 50 ° C at 1 bar and mixtures the said gases.
- Particularly preferred are carbon dioxide, ethane, propane or butane.
- the compressed gas is carbon dioxide or propane.
- Propane and carbon dioxide have a particularly favorable for the purposes of the invention Joule-Thompson effect and evaporate well from the shell, so that at most only small contaminants remain.
- spray-drying may also be carried out, precipitation from suitable solvents or alternative high-pressure spraying processes may be used.
- the method according to the invention has the advantage that no solvent is used which subsequently has to be separated off or contaminates the particles. Compared with spray drying, lower working temperatures result since, for example, the use of carbon dioxide lowers the melting temperature of the mixture and its viscosity.
- Other high-pressure processes usually work with higher carbon dioxide and energy requirements, so they are less economical in this case.
- the step of charging the melt with gas is preferably carried out at a pressure in the range of 100 to 200 bar. Further, the temperature in this step is preferably in the range of 25 to 80 0 C.
- the nozzles or capillaries of the PGSS system preferably have a diameter in the range of 50 ⁇ m to 1500 ⁇ m.
- the capsule material and the additives are melted and the viruses are dispersed in the melt.
- the melt is charged with carbon dioxide, the pressure between 20 and 500 bar (preferably 100-200 bar) is selected and the temperature between 10 0 C and 100 0 C (preferably 25 ° C to 65 ° C) is set , but at least so high that the capsule material melts. Temperature and dwell time are chosen so that the viruses are not deactivated.
- the capsule material is sprayed with the dissolved carbon dioxide through a nozzle or capillary (diameter between 50 microns and 1500 microns, preferably 200 - 500 microns). The resulting particles are collected.
- 150 g capsule material (.. 80 wt% tripalmitin, 20% by weight of palmitic) are melted at 60 0 C and (4 ml of a glycerol-containing codling moth Granulovirus suspension available under the trade name Madex; virus concentration about 3 x 10 13 viruses per liter ).
- the mixture is introduced in a pressure vessel with stirrer.
- the temperature of the melt is maintained at 60 ° C and it is added via a compressor carbon dioxide, so that a pressure of 100 bar sets and stirred for 30 min.
- a nozzle connected to the container 60 ° hollow cone nozzle, 400 microns
- the mean size of the capsules obtained is 15 ⁇ m.
- the calculated load is 1, 25 viruses per capsule.
- Viruses heated to 65 ° C for 1 h have an efficiency of 95% compared to thermally untreated viruses. At 70 0 C heated viruses still have an efficiency of about 88%, at 80 0 C heated viruses kill only 30% of the larvae.
- microparticles prepared by the above method showed in animal experiments an efficiency of over 88%, based on unencapsulated viruses.
- the encapsulated viruses showed an improved efficiency compared to untreated viruses, indicating both improved UV stabilization and increased uptake rates.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Virology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Dispersion Chemistry (AREA)
- Microbiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Medicinal Preparation (AREA)
Abstract
La présente invention concerne des microparticules encapsulées présentant un noyau qui contient des virus sous une forme libre ou liée à un support, et une enveloppe qui entoure le noyau. Les microparticules se caractérisent en ce que l'enveloppe se compose à au moins 50 % en poids d'un ou de plusieurs triacylglycérides dont la chaîne d'acides aminés mesure de C10 à C24.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007057395A DE102007057395A1 (de) | 2007-11-27 | 2007-11-27 | Verkapselte Mikropartikel mit einem virenhaltigen Kern und Verfahren zur Herstellung der Mikropartikel |
| PCT/EP2008/065752 WO2009068458A2 (fr) | 2007-11-27 | 2008-11-18 | Microparticules encapsulées présentant un noyau qui contient des virus, et procédé de préparation des microparticules |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2217362A2 true EP2217362A2 (fr) | 2010-08-18 |
Family
ID=40577160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP08854538A Withdrawn EP2217362A2 (fr) | 2007-11-27 | 2008-11-18 | Microparticules encapsulées présentant un noyau qui contient des virus, et procédé de préparation des microparticules |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP2217362A2 (fr) |
| DE (1) | DE102007057395A1 (fr) |
| WO (1) | WO2009068458A2 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010037140A1 (de) * | 2010-08-24 | 2012-03-01 | EuroFerm Gesellschaft für Fermentation und Messtechnik mbH | Verfahren zum Schutz von Pflanzen |
| DE102010037141A1 (de) * | 2010-08-24 | 2012-03-01 | EuroFerm Gesellschaft für Fermentation und Messtechnik mbH | Pflanzenschutzmittel enthaltend insektenpathogene Viren, insbesondere Baculoviren und Zellulosesulfat |
| CN107232190B (zh) * | 2017-05-31 | 2021-04-27 | 中国农业科学院植物保护研究所 | 噻虫胺控释包埋颗粒剂及其制备和应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1272943B (it) * | 1994-02-01 | 1997-07-01 | Bend Res Inc | Composizioni insetticide labili |
| AU5670096A (en) * | 1995-05-25 | 1996-12-11 | Biotechnology Research And Development Corporation | Casein-based sprayable formulation for pest control |
| WO1998015183A1 (fr) * | 1996-10-07 | 1998-04-16 | E.I. Du Pont De Nemours And Company | Procede permettant d'enrober des pesticides biologiques et compositions contenant lesdits pesticides |
| US6506397B1 (en) * | 1999-02-19 | 2003-01-14 | Curt Thies | Pest controlling |
| US6248363B1 (en) * | 1999-11-23 | 2001-06-19 | Lipocine, Inc. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| US6720001B2 (en) * | 1999-10-18 | 2004-04-13 | Lipocine, Inc. | Emulsion compositions for polyfunctional active ingredients |
| US6365189B1 (en) * | 1999-10-22 | 2002-04-02 | 3M Innovative Properties Company | Method of delivering and releasing a pheromone |
| US20030180352A1 (en) * | 1999-11-23 | 2003-09-25 | Patel Mahesh V. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| WO2005005010A2 (fr) * | 2003-02-21 | 2005-01-20 | Ferro Corporation | Procedes et appareil de production de particules composites utilisant un fluide supercritique comme agent plastifiant et d'extraction |
| US20050084513A1 (en) * | 2003-10-21 | 2005-04-21 | Board Of Regents | Nanocoating for improving biocompatibility of medical implants |
| US20040224019A1 (en) * | 2004-03-03 | 2004-11-11 | Adi Shefer | Oral controlled release system for targeted drug delivery into the cell and its nucleus for gene therapy, DNA vaccination, and administration of gene based drugs |
-
2007
- 2007-11-27 DE DE102007057395A patent/DE102007057395A1/de not_active Ceased
-
2008
- 2008-11-18 EP EP08854538A patent/EP2217362A2/fr not_active Withdrawn
- 2008-11-18 WO PCT/EP2008/065752 patent/WO2009068458A2/fr not_active Ceased
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2009068458A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009068458A2 (fr) | 2009-06-04 |
| DE102007057395A1 (de) | 2009-05-28 |
| WO2009068458A3 (fr) | 2009-08-20 |
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