WO2022146242A1 - Composition d'une hémoculture bioadsorbante chargée de nanoparticules et son procédé de production - Google Patents
Composition d'une hémoculture bioadsorbante chargée de nanoparticules et son procédé de production Download PDFInfo
- Publication number
- WO2022146242A1 WO2022146242A1 PCT/TR2020/051429 TR2020051429W WO2022146242A1 WO 2022146242 A1 WO2022146242 A1 WO 2022146242A1 TR 2020051429 W TR2020051429 W TR 2020051429W WO 2022146242 A1 WO2022146242 A1 WO 2022146242A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- nanoparticle
- blood culture
- production method
- cellulose
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 238000009640 blood culture Methods 0.000 title claims abstract description 37
- 239000002105 nanoparticle Substances 0.000 title claims abstract description 35
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 20
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 54
- 229910052742 iron Inorganic materials 0.000 claims abstract description 27
- 240000008886 Ceratonia siliqua Species 0.000 claims abstract description 19
- 239000001913 cellulose Substances 0.000 claims abstract description 19
- 229920002678 cellulose Polymers 0.000 claims abstract description 19
- 235000013912 Ceratonia siliqua Nutrition 0.000 claims abstract description 18
- 241000717739 Boswellia sacra Species 0.000 claims abstract description 16
- 241001519020 Cassia brewsteri Species 0.000 claims abstract description 15
- OAQWWRSICWQQSE-UHFFFAOYSA-N octan-2-yl 16-methylheptadecanoate Chemical compound CCCCCCC(C)OC(=O)CCCCCCCCCCCCCCC(C)C OAQWWRSICWQQSE-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 14
- 239000004863 Frankincense Substances 0.000 claims abstract description 13
- 235000013399 edible fruits Nutrition 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 29
- 239000003463 adsorbent Substances 0.000 claims description 22
- 241000196324 Embryophyta Species 0.000 claims description 10
- 239000002086 nanomaterial Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000008131 herbal destillate Substances 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 5
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 238000001704 evaporation Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims description 2
- 238000000605 extraction Methods 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 238000010257 thawing Methods 0.000 claims description 2
- 238000002525 ultrasonication Methods 0.000 claims description 2
- 244000020551 Helianthus annuus Species 0.000 claims 1
- 230000018044 dehydration Effects 0.000 claims 1
- 238000006297 dehydration reaction Methods 0.000 claims 1
- 230000003115 biocidal effect Effects 0.000 abstract description 14
- 206010040047 Sepsis Diseases 0.000 abstract description 8
- 239000003242 anti bacterial agent Substances 0.000 description 8
- 229940088710 antibiotic agent Drugs 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 244000052769 pathogen Species 0.000 description 6
- 239000012153 distilled water Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000018109 developmental process Effects 0.000 description 4
- 208000015181 infectious disease Diseases 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241001608538 Boswellia Species 0.000 description 3
- 235000018062 Boswellia Nutrition 0.000 description 3
- 241000208818 Helianthus Species 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 230000001717 pathogenic effect Effects 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 235000017367 Guainella Nutrition 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000008055 phosphate buffer solution Substances 0.000 description 2
- 150000008442 polyphenolic compounds Chemical class 0.000 description 2
- 235000013824 polyphenols Nutrition 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 208000035473 Communicable disease Diseases 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 239000007836 KH2PO4 Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 206010053159 Organ failure Diseases 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 229940127090 anticoagulant agent Drugs 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000008366 buffered solution Substances 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- -1 collodion Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 230000000004 hemodynamic effect Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000004768 organ dysfunction Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002338 polyhydroxyethylmethacrylate Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 125000004402 polyphenol group Chemical group 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012256 powdered iron Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
- C12Q1/04—Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/02—Cellulose; Modified cellulose
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/26—Infectious diseases, e.g. generalised sepsis
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54313—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being characterised by its particulate form
- G01N33/54346—Nanoparticles
Definitions
- the invention relates to a composition of a nanoparticle loaded bio adsorbent blood culture and the production method of the said composition for use in the health sector in defining the microbiological etiology in suspected infection cases.
- Sepsis is a fatal infectious disease that involves many systems, especially causing hemodynamic changes, leading to shock, organ dysfunction, and organ failure.
- the survival rate of the patients who have bacteria in their blood and treated with antibiotics within the first 2 hours is 80 %, while in patients who started antibiotics after 12 hours, this rate drops by almost half.
- the pathogen detection rate in blood cultures has been increased with new methods. Examples of these are the development of new mediums, the addition of growth factors to the mediums, and the neutralization of growth inhibitors I metabolic products I antibiotic residues.
- the average positivity period of automated blood culture measurement systems and bottles is 5 - 7 days, and for other systems, the average is 15 hours.
- the value of conventional blood cultures is limited in slow or difficult breeds or in species that cannot be cultured and its sensitivity decreases in those who take antibiotic treatment and when the burden of microorganisms is low.
- the false - positive blood cultures cause results to be interpreted with error, resulting in the incorrect use of antibiotics, additional laboratory tests, prolonged hospital stay and increased examination and treatment costs.
- Sepsis patients are given high doses of antibiotics.
- the blood taken from the patient is kept in a medium containing the nutrients of the pathogens that cause the infection, and pathogen growth is observed.
- the blood taken from the patient due to antibiotic treatment can suppress these pathogens for a period of time, and the amount of growth appears to be lower than it should be, or there are certain deviations.
- the BACTEC blood culture system (BD Diagnostics) produced for this purpose consists of an antibiotic binding resin on small glass beads, while the BacT / Alert blood culture system (BioMerieux Inc.) uses activated charcoal powder.
- it is aimed to retain the antibiotic with the material chosen as adsorbent.
- a patent application document numbered US4543328A is found.
- the said document describes a process and device for the detection of pathogens, such as bacteria, fungi, and viruses, in blood in the presence of an anticoagulant agent.
- the polymer is selected from the group of polyacrylate, polymethacrylate, polyhydroxy ethyl methacrylate, an adsorber resin, synthetic crosslinked polystyrene, cellulose acetate, collodion, and nylon.
- the present invention relates to a composition of a nanoparticle loaded bio adsorbent blood culture and its production method that meets the above - mentioned requirements, eliminates all disadvantages, and brings some additional advantages.
- the main purpose of the invention is to develop a new blood culture composition, especially for use in the examinations of sepsis patients.
- the quality of the examination is improved, and the duration of the examination is shortened.
- early precautions can be taken by obtaining rapid results in the treatment of fatal sepsis patients.
- the blood culture composition of the invention contains bioadsorbent material charged with iron nanoparticles obtained through herbal synthesis.
- a mixture comprising of the fruit and seeds of carob bean tree (Ceratonia siliqua), shell and resin of the olibanum (Boswellia carterii), as well as cellulose and flower - shaped iron hybrid nanostructure are used.
- hydrosol obtained from the selected plant combinations as the reducing material is sufficient. It was determined that the composition containing the flower - shaped iron hybrid nanoparticle obtained using plant hydrosol not only retains the antibiotic in the environment but breaks it down, disrupting its structure.
- Another object of the invention is to demonstrate that there is no need to use chemicals as reducers and stabilizers as in the current technique since the use of plant hydrosols is sufficient to obtain nanoparticles.
- composition of the invention all reducing, stabilizing agents are composed of plant - derived raw materials.
- biomaterial synthesis nano iron solution due to the herbal synthesis nano iron solution, the antibiotic adhesion surface area, and the rate of degradation of the antibiotic are increased.
- the resin used in state of the art has a narrower surface area than nanoparticles, so it reaches saturation in a shorter time, and its performance decreases.
- the antibiotics, which cannot be retained by resin give misleading results in diagnosis. Since the antibiotic in the environment is not only retained but also degraded employing the invention, the aforementioned problems can be avoided.
- the invention comprises flower - shaped iron hybrid nanostructure and cellulose obtained using the fruit and seeds of carob bean tree and shell and resin of the Olibanum.
- the cellulose charged with flower - shaped iron hybrid nanoparticles synthesized by herbal methods in the scope of the invention can be easily applied to any environment in which human contact is made and is environmentally friendly.
- the innovative aspects of the product of the invention are listed below;
- the antibiotic is adsorbed, and together with the deterioration of its structure, its effect is completely eliminated
- Figure 1 shows The SEM image of plant synthesis flower - shaped iron hybrid nanostructure.
- Figure 2 shows The TEM image of iron nanoparticles that form the center of the flower - shaped hybrid nanostructure.
- Figure 3 shows the results of EDX analysis.
- Figure 4 shows the results of FT - IR analysis.
- Figure 5 shows the results of BET surface area analysis.
- the invention relates to the composition of a nanoparticle - charged bioadsorbent blood culture and the production method of the said composition for use in determining the state of antibiotic administration.
- the said blood culture composition comprises the fruit and seeds of carob bean tree and shell and resin of the Olibanum, iron, and cellulose.
- Olibanum (Boswellia carterii) resin contains ester and acidic components and has high antimicrobial properties. In the composition of the invention, it is combined with carob bean tree hydrosols in the appropriate proportion to the composition, providing a flower - shaped organic - inorganic hybrid structure.
- the carob bean tree (Ceratonia siliqua L.) plant contains a high percentage of polyphenols in its fruit.
- the polyphenol group consists of carbohydrates (48 - 56 %), condensate tannin (16 - 20 %).
- Polyphenols can reduce metals by forming complexes with metal ions.
- Olibanum hydrosols in the appropriate proportion to the composition, providing a flower - shaped organic - inorganic hybrid structure.
- composition of the invention in its most basic form, comprises the following steps;
- the structure of the nanoparticle loaded bio adsorbent blood culture composition of the invention comprises, by weight
- blood culture composition preferably comprises, by weight
- the resulting iron nanoparticle loaded cellulose - based adsorbent material is added to existing blood culture bottles in the appropriate proportion instead of resin or activated carbon.
- the invention is a blood culture composition containing carob bean tree and olibanum plant hydrosols, the iron, and cellulose.
- the invention is a blood culture composition production method, characterized by comprising the following process steps of i. Preparation of the PBS solution ii. Obtaining of hydrosols of the fruit and seeds of carob bean tree, shell and resin of the olibanum in the PBS, iii. Thawing of iron, iv. Combining iron thawed in step (iii) and plant hydrosols treated with PBS in step (ii), v. Extraction of cellulose from sunflower heart and stem pulp, vi. Evaporation of the water of the mixture obtained in the process step (iii), vii. Charging the powdered iron nanoparticle obtained in the process step (vi) into the cellulose adsorbent obtained in the process step (iv).
Abstract
L'invention concerne une composition d'hémoculture contenant des fruits et des graines de caroubier, de la résine et de la coque d'oliban, des nanoparticules de fer et de la cellulose, et le procédé de production de ladite composition, destinée à être utilisée pour déterminer l'état de l'administration d'antibiotiques dans le traitement de la septicémie dans le secteur de la santé.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/TR2020/051429 WO2022146242A1 (fr) | 2020-12-29 | 2020-12-29 | Composition d'une hémoculture bioadsorbante chargée de nanoparticules et son procédé de production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/TR2020/051429 WO2022146242A1 (fr) | 2020-12-29 | 2020-12-29 | Composition d'une hémoculture bioadsorbante chargée de nanoparticules et son procédé de production |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2022146242A1 true WO2022146242A1 (fr) | 2022-07-07 |
Family
ID=82259598
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/TR2020/051429 WO2022146242A1 (fr) | 2020-12-29 | 2020-12-29 | Composition d'une hémoculture bioadsorbante chargée de nanoparticules et son procédé de production |
Country Status (1)
Country | Link |
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WO (1) | WO2022146242A1 (fr) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4543328A (en) * | 1978-06-16 | 1985-09-24 | Boehringer Mannheim Gmbh | Process for detecting pathogens |
CN104928240A (zh) * | 2015-07-01 | 2015-09-23 | 浙江元太生物科技有限公司 | 一种自体或异体红细胞培养基的制备方法 |
CN106479931A (zh) * | 2016-11-04 | 2017-03-08 | 哈尔滨亿隆科技有限公司 | 一种血琼脂培养基的改良配方 |
-
2020
- 2020-12-29 WO PCT/TR2020/051429 patent/WO2022146242A1/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4543328A (en) * | 1978-06-16 | 1985-09-24 | Boehringer Mannheim Gmbh | Process for detecting pathogens |
CN104928240A (zh) * | 2015-07-01 | 2015-09-23 | 浙江元太生物科技有限公司 | 一种自体或异体红细胞培养基的制备方法 |
CN106479931A (zh) * | 2016-11-04 | 2017-03-08 | 哈尔滨亿隆科技有限公司 | 一种血琼脂培养基的改良配方 |
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