504results about How to "Increased drug resistance" patented technology

The invention discloses a botanical plant protection agent, whose raw material components and parts by weight include: 1-3 parts of litsea cubeba oil, 1-8 parts of azadirachtin, 3-5 parts of silicate, 0.5 parts of surfactant -1 part, 5-10 parts of tackifier and 500-700 parts of water. The preparation method comprises the steps of dissolving the tackifier raw material with water to form a tackifier solution, then emulsifying the litsea cubeba oil and azadirachtin with water, adding the tackifier solution solution and silicate, fully stirring and mixing uniformly to obtain the product . The botanical plant protection agent of the present invention maintains the characteristics of low toxicity, high efficiency, easy degradation, and no residue of botanical pesticides, is not easy to produce drug resistance to pests, does not pollute the environment, and has a good control effect on crops. It is a broad-spectrum new pesticide preparation for pest, sterilization and anti-virus, which can be used alone or/and mixed with common insecticides and pesticides.

The invention relates to a manufacturing method of a container cup and a structure thereof, which belongs to the daily article class. The invention comprises a paper cup and a cup-shaped electronic bridging foaming body, wherein the inner surface or the outer surface of the paper cup is sprinkled and covered with a film layer, and is pressed into the paper cup through shape cutting; the cup-shaped electronic bridging foaming body is formed by being bonded in a hot pressing way after an electronic bridging foaming plate is manufactured into a sector body through printing, shape cutting and stripe pinching, the inner peripheral of the cup-shaped electronic bridging foaming body is ensured to produce softening viscosity in the hot pressing way, then the paper cup is directly covered on and bonded with the inside of the cup-shaped electronic bridging foaming body, and meanwhile a convex ring with a oversize diameter is formed at the outer part of the paper cup lip where the cup-shaped electronic bridging foaming body is positioned. The structure has the advantages that the protective effect is good, the thermal insulation function is good, the water absorbability is low, the appearance is smooth and artistic, the structure is not easy to be metamorphic, the drug fastness is good, the processing is easy, etc.

The invention relates to use of a 2-mercaptobenzothiazole metal salt, and especially provides a crop disease prevention and treatment bactericide. The bactericide is characterized in that the bactericide includes the 2-mercaptobenzothiazole metal salt represented by formula (I) and a pesticide carrier; and in the formula (I), M is Zn, Mn, Fe, Sn or Al, and n is 2, 3 or 4. The bactericide has a very high biological activity against most bacteria and an excellent inhibition effect on fungi, and is an ideal drug for comprehensively preventing and treating diseases of crops.

The present invention relates to a cement-free alkali activated binder in which alkaline inorganic materials are appropriately added to an industrial waste such as blast furnace slag, fly ash, meta kaolin and the like, a method for producing mortar using the same and a method for producing cement-free alkali activated reinforcement mortar. Specifically, the present invention relates to a cement-free alkali activated binder that is not only environmentally friendly as being capable of dramatically reducing the carbon dioxide emission, which has been remained as a problem for producing Portlandcement, but also has an excellent property, a method for producing mortar using the same and a method for producing cement-free alkali activated reinforcement mortar.

The invention relates to novel hydrazide derivatives as well as a preparation method and application thereof. The novel hydrazide derivatives have a general formula as shown in the specification, wherein each group is as shown in the claim 1. The novel hydrazide derivatives provided by the invention are improved in insecticidal activity while the previous compound lipid solubility thereof is improved; the derivatives have excellent insecticidal activity; instantly after the derivatives are applied, insects can lose control on muscle and stop eating, and are obviously shrank and paralyzed; at last, the insects can be caused to die, and in the meantime, abnormal ecdysis of insects also can be induced; the novel hydrazide derivatives are very effective especially for lepidoptera pests such as mythimna separata, plutella xylostella and asparagus caterpillar, and thus are pesticides having wide application prospect.

The invention relates to the field of agricultural fungicide, in particular to a botanical fungicide, an extracting method and the usage thereof. The botanical fungicide adopts extracts of plant raw materials such as sisal leaves, wild chrysanthemum, Chinese parasol leaves, ginger, bitter gourd or the like; the original preparation technology is improved, and the botanical fungicide is used for controlling agricultural diseases and has good environmental compatibility; the three-time extracting technique is adopted, and ultrasound-assisted extraction is applied, so that the maximum extraction capacity of active ingredient can be ensured; the technique is simple and seldom affects the environment, and the extracts have good effect on sterilization and bacteriostasis.

The method discloses a mouth rinse for removing halitosis and a preparation method thereof. The mouth rinse for removing halitosis comprises nidazole medicines, Chinese herbal medicine extracts, menthol, glycerin, a surface active agent and deionized water. In the invention, the mouth rinse for removing halitosis takes the nidazole medicines as a main therapeutic ingredient, and enhances therapeutic effect by adding the Chinese herbal medicine extracts for health care. Compared with the mouth rinse with a single active ingredient, the mouth rinse of the invention can be applicable to more indications, has more obvious therapeutic effect on removing oral abnormal odor, can effectively improve oral inflammation without destroying normal oral floras, and has the advantages of short use time, good drug resistance, convenient use, good mouth feel and easy acceptance of patients.

The invention discloses an anti-tumor combination and the application thereof; the anti-tumor combination which includes effective dose of platinum-based chemotherapy and AKT inhibitor and / or p70S6K1 inhibitor has the function of inhibiting the drug resistance of the tumor to the platinum-based chemotherapy, improves the effects of anti-tumor drugs, and can be used for preparing drugs that can resist various tumors, such as lung cancer, ovarian cancer, prostate cancer, breast cancer, stomach cancer, nasopharyngeal cancer, esophageal cancer, malignant lymphoma, head and neck squamous cell carcinoma, thyroid cancer, osteosarcoma, etc.

The invention relates to a multidrug resistant cell strain for oophoroma, which is characterized in that a human oophoroma SKOV3 cell strain is selected as a parental cell; the action concentration of chemotherapeutics of etoposide (VP16) is gradually increased from 0.1 mu g/ml to 3 mu g/ml; and drug resistant SKOV3/VP16 cell strain is established. The SKOV3/VP16 cell can stably grow, transfer and reanimate in 3 mu g/ml VP16, makes the VP16 generate drug resistant index (RI) of 21.548, and performs intersect drug on MTX, DOX, DDP, VCR, 5-Fu and MMC except the VP16. The invention aims to provide a drug resistant tumor cell model for relative study on the tumor.

The invention relates to a multiple-gene helicobacter pylori detection system and a kit and application thereof. The helicobacter pylori detection system includes 21 pairs of primers respectively for a strain identification gene (16S rRNA), virulence genes (cagA, vacA-s1, vacA-s2, vacA-m1, vacA-m2, iceA1, iceA2, dupA, oipA and luxS), drug resistance genes (2143 locus of 23S rRNA, 148 locus of rdxA, 1777 locus of pbp1A and polymorphism of the 261 locus of gyrA) and quantitative analysis genes ureC and beta-globin of the helicobacter pylori. The multiple-gene helicobacter pylori detection system and the kit of the system do not need the steps including conventional isolated culture and the like, synchronous detection and analysis on strain identification, quantification, virulence and medicine resistance can be directly conducted on tissue samples in the same reaction system, the shortcomings of low flux, long consumed time, low detection rate and the like of a conventional detection method are overcome, a comprehensive, accurate and low-cost etiological diagnosis is clinically provided for the first time, and important references are provided for individualized diagnosis and accurate treatment of helicobacter pylori infection.

A copper conductor sizing agent is able to form a copper conductor film which the atmosphere be controlled to obtain a high density force while not strictly sintering, and less reduction of the density force because of the plating process. The copper conductor sizing agent contains conductive powder with the core of the copper powder, the first glass melting material which is helpful for enhancing the wetting quality, the second glass melting material which is helpful for enhancing resistance to chemical reagents, organic medium. (1) the first glass melting material, the softening point is below 800 centigrade, in the nitrogen atmosphere at 900 centigrade, the contact angle corresponding to the copper powder which is not oxidized superficially is below 60 degrees; (2) the solubility of the second glass melting material is below 1mg/cm2hr corresponding to the 10 quality% sulphuric acid aqueous solution at 25 centigrade; (3) the difference between the softening point of the first glass melting material and the softening point of the second glass melting material is below 150 centigrade; (4) relevant to the total quantity of the glass melting material, the content of the first glass melting material is 10-70 quality%; the content of the second glass melting material is 30-90 quality%.

The invention relates to novel chloroethyl nitrosourea with anticancer activity and a synthesizing method thereof. The chloroethyl nitrosourea is a compound with a structure of the general formula (I), wherein n is an integer of 2 to 6. The chloroethyl nitrosourea can be used for treating gliomatosis cerebri, colon cancer and leukemia; compared with the existing nitrosourea-type anticancer medicine, the drug resistance is lower, the chemical therapy effect is better, the preparation method is simple in operation, the reaction yield is high, the toxicity is small, the cost is low, the method is suitable for the industrialized production, the development prospect is wide, and the application value is good.

The invention relates to an urethanated unsaturated water-soluble vinyl multipolymer and a preparation method thereof. The urethanated unsaturated water-soluble vinyl multipolymer is a vinyl multipolymer containing the following structure unit: -A-B-C (-X)-D-, wherein A represents a styrene structure unit; B represents a (methyl) acrylonitrile structure unit; C represents a vinyl copolymerization unit containing branched hydroxyl; D represents a vinyl copolymerization unit containing a branched hydrophilic group; and X represents a C unit branched hydroxyl grafted unsaturated mono isocyanate structure unit. The polymer is applicable to manufacturing chemistry-free CTP boards.

The invention discloses a nano antibacterial agent and a preparation method thereof and relates to an antibacterial agent and a preparation method thereof. The invention aims to solve the problems that the conventional nanometer material modified antibiotics applied to the antibacterial field have poor biocompatibility and do not have targeting property and the utilization rate of the antibioticsis low. The nano antibacterial agent is prepared by performing surface modification on a synergetic system of MOF and antibiotics with sodium hyaluronate, wherein the synergetic system of the MOF andantibiotics with sodium hyaluronate is formed by encapsulating the antibiotics in a zeolite imidazate framework structure material ZIF-8. The method comprises the following steps: 1, preparing the synergetic system of the MOF and antibiotics; 2, performing surface modification on the prepared synergetic system of the MOF and antibiotics with a sodium hyaluronate solution, and performing vacuum drying, thereby obtaining the nano antibacterial agent. According to the preparation method disclosed by the invention, the nano antibacterial agent can be obtained.