Thursday, August 29, 2013
Sulfaclozine Sodium Uses
Purpose:
(1) poultry, poultry coccidiosis Sulfachloropyrazine role characteristics and similar Sulfaquinoxalinum, and possessed a stronger antibacterial effect, and even treat fowl cholera and fowl typhoid, so the most suitable for treatment with the outbreak of coccidiosis .
Application Sulfachloropyrazine not affect the host immunity against coccidiosis.
(2) Other This product is also quite effective coccidiosis free, can be used per 1000kg feed, add 600g Sulfachloropyridazine adjacent triazine sodium, and even fed 5 to 10 days.
On lamb coccidiosis, each lkg body weight, can be 3% solution 1.2mL orally, once every 3 to 5 days.
Note:
(1) This product is far more toxic Sulfaquinoxalinum low, but the long-term application still appears sulfa drug poisoning symptoms, so chickens can only be recommended concentrations, once every three days, to a maximum of 5 days.
(2) In view of the majority of our farms, the application of sulfa drugs (such as SQ, SM2, etc.) has been for decades, coccidia sulfonamide resistance may have even cross-resistance, so that in case of poor efficacy phenomenon, should be replaced drugs.
(3) more than 16 weeks of laying hens and chickens disabled.
(4) the withdrawal period, turkeys 4 days broiler one day.
More about:Sulfaclozine Sodium manufacturer
From:Natural herbal extracts
Tuesday, August 27, 2013
L-Cystine introduction of related purposes
L-cystine is a nutritional supplement. For milk breast milk. Is a non-essential amino acids. Constitute the skin and hair is essential substances, can promote surgery and trauma treatment. Stimulate hematopoietic function, and promote leukocyte formation. Promote oxidation of body cells and restore function, but also can be used for cosmetic additives can promote wound healing, prevention and treatment of eczema and other allergic skin effect.
Purpose:
1 for biochemical research. Preparation of biological medium. For biochemistry and nutrition research, medicine can promote oxidation of body cells and restore function, increased white blood cells and prevent pathogen growth and so on. Mainly used for a variety of alopecia. Also used for dysentery, typhoid, influenza and other acute infectious diseases, asthma, neuralgia, eczema and various diseases such as poisoning, and to maintain the role of protein conformation. Also used as a food flavoring agent.
(2) biochemical reagents for biological media preparation. Amino acid infusion and also an important component of the composite amino acid preparations
3 for nutritional supplements, is conducive to animal development, weight gain, and liver and kidney function, improve the quality of fur.
4 can be used for cosmetic additives, can promote wound healing and prevent skin allergies and eczema and so on.
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From:Natural herbal extracts
Sunday, August 25, 2013
Arimadex (Anastrozole) pharmacy medical knowledge
Arimadex (Anastrozole) tablets tradename Rui Ting, Arimidex, is a potent non-steroidal aromatase inhibitors. May reduce plasma levels of estrogen, resulting in inhibition of mammary tumor growth. Clinic for postmenopausal women with advanced breast cancer.
Product Use:
Use one: potent and selective aromatase inhibitors triazole, can inhibit the cytochrome P-450 enzyme aromatase depend thereby blocking the biosynthesis of estrogen, and estrogen to stimulate the growth of breast cancer cells the main factor.
Uses two: the treatment of breast cancer, especially for those with hormone relapse after adjuvant therapy in women after menopause advanced breast cancer.
Pharmaceutical medical knowledge:
Indications: For anastrozole after tamoxifen and other anti-estrogen therapy still can not control in postmenopausal women with advanced breast cancer. On estrogen receptor-negative patients, if their right tamoxifen showed positive clinical response, consider using anastrozole.
ACTION: Anastrozole is a potent and selective non-steroidal aromatase inhibitors. Inhibit postmenopausal patients with adrenal androstenedione generated into estrone, which significantly reduced plasma levels of estrogen, resulting in inhibition of mammary tumor growth. In addition, anastrozole right adrenal corticosteroids or aldosterone generate no significant effect.
Pharmacokinetics: oral anastrozole absorbed quickly in the body about 40% of anastrozole and plasma protein binding, the majority metabolized into inactive products were excluded from the urine, about 10 per cent of the prototype anastrozole excluded from the urine . According to reports, healthy male volunteers after oral administration of 1mg, time to peak plasma concentration was 1.22 ± 0.46 hours, peak plasma concentration was 9.99 ± 3.24ng/ml, elimination half-life of 35.96 ± 14.17 hours.
Dosage: Tablets: orally once a day, every one (1 mg), with mild to moderate hepatic function or mild renal impairment in patients with generally Needless to adjust the dose.
More about:Arimadex (Anastrozole) manufacturer
From:Natural herbal extracts
Product Use:
Use one: potent and selective aromatase inhibitors triazole, can inhibit the cytochrome P-450 enzyme aromatase depend thereby blocking the biosynthesis of estrogen, and estrogen to stimulate the growth of breast cancer cells the main factor.
Uses two: the treatment of breast cancer, especially for those with hormone relapse after adjuvant therapy in women after menopause advanced breast cancer.
Pharmaceutical medical knowledge:
Indications: For anastrozole after tamoxifen and other anti-estrogen therapy still can not control in postmenopausal women with advanced breast cancer. On estrogen receptor-negative patients, if their right tamoxifen showed positive clinical response, consider using anastrozole.
ACTION: Anastrozole is a potent and selective non-steroidal aromatase inhibitors. Inhibit postmenopausal patients with adrenal androstenedione generated into estrone, which significantly reduced plasma levels of estrogen, resulting in inhibition of mammary tumor growth. In addition, anastrozole right adrenal corticosteroids or aldosterone generate no significant effect.
Pharmacokinetics: oral anastrozole absorbed quickly in the body about 40% of anastrozole and plasma protein binding, the majority metabolized into inactive products were excluded from the urine, about 10 per cent of the prototype anastrozole excluded from the urine . According to reports, healthy male volunteers after oral administration of 1mg, time to peak plasma concentration was 1.22 ± 0.46 hours, peak plasma concentration was 9.99 ± 3.24ng/ml, elimination half-life of 35.96 ± 14.17 hours.
Dosage: Tablets: orally once a day, every one (1 mg), with mild to moderate hepatic function or mild renal impairment in patients with generally Needless to adjust the dose.
More about:Arimadex (Anastrozole) manufacturer
From:Natural herbal extracts
Thursday, August 22, 2013
Tranexamic Acid pharmacological effects
Tranexamic Acid Chemical name: aminomethylcyclohexane acid, trans-4 - (aminomethyl) - cyclohexane carboxylic acid. Mainly used for acute or chronic, localized or systemic fibrinolysis hyperthyroidism caused by a variety of bleeding. Disseminated intravascular coagulation due to high secondary fibrinolysis, in the absence of heparin, before, careful.
Pharmacological effects:
Fibrinolytic phenomenon and the body under physiological or pathological state fibrinolytic, increased vascular permeability, etc., but also with fibrinolysis induced reaction of the organism, such as a variety of bleeding symptoms and the incidence of allergy associated with the development and healing. This product can inhibit plasmin role, and show bleeding, anti-allergic, anti-inflammatory effect.
1 antifibrinolytic action of enzymes
Tranexamic acid to plasmin and plasminogen with fibrin on the part of the lysine affinity binding site (LBS) is strongly adsorbed, inhibition of plasmin, plasminogen and fibrin binding and thus strongly inhibit fibrin by plasmin induced decomposition; addition, serum macroglobulin and other anti-plasminogen in the presence of tranexamic acid antifibrinolytic effect is more obvious
Pharmacokinetic properties: bioavailability of 34%, half-life of 3.1h
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From:Natural herbal extracts
Tuesday, August 20, 2013
BM-MSCs separation method
BM-MSCs are bone marrow stem cells, bone marrow hematopoietic stem cells (HSC) is not only mechanical support role, but also secrete a variety of growth factors (such as IL-6, IL-11, LIF, M-CSF and SCF, etc.) to support hematopoiesis.
MSC currently used methods include separation of whole bone marrow and density gradient centrifugation method that is based on whole bone marrow stem cells in low serum medium planted with adherent edge features, the medium was changed regularly adherent cells are not removed, so as to achieve purification and expansion MSC additional purposes. Density gradient centrifugation of the cells in the bone marrow that are based on the proportion of different components, mononuclear cells adherent culture. Essentially no much difference between the two. With in-depth understanding of MSC surface antigen, and anyone using immunological methods such as flow cytometry, immunofluorescence beads, etc. be isolated and purified. But after flow sorting or magnetic bead cell appeared after some problems such as slow growth, coupled with the high cost and technical difficulty, to some extent limited the widespread application of these methods.
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From:Natural herbal extracts
Tuesday, August 13, 2013
Amiodarone Hydrochloride traits and uses
Appearance: white to light yellow crystalline powder, almost odorless, tasteless, melting point 153 ~ 158 ℃. Soluble in chloroform, soluble in ethanol, slightly soluble in acetone, insoluble in water.
Action and Uses: Amiodarone Hydrochloride for the anti-angina drugs can selectively dilating coronary blood flow, while reducing myocardial oxygen consumption, heart rate, atrioventricular conduction velocity decreased with β-blockers similar effect. For supraventricular and ventricular tachycardia, paroxysmal atrial fibrillation and flutter, WPW syndrome, but also for chronic paroxysmal tachycardia, coronary insufficiency and angina pectoris.
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From:Natural herbal extracts
Monday, August 12, 2013
Ertapenem Sodium for injection some indications
Indications: Ertapenem Sodium for the treatment of adults by the following bacteria caused by susceptible strains of the following moderate to severe infections. (See DOSAGE AND ADMINISTRATION) · secondary abdominal infections: Escherichia coli, Clostridium, slow Eubacterium, Peptostreptococcus, Bacteroides fragilis, Bacteroides Gibbs, B. ovatus, Bacteroides thetaiotaomicron or simplex caused by Bacteroides. · Complicated skin and appendages infections: Staphylococcus aureus (methicillin-susceptible strains only refers to), Streptococcus pyogenes, Escherichia coli, or those caused by Peptostreptococcus. • Community-acquired pneumonia: Streptococcus pneumoniae (penicillin-susceptible strains only refer to, including the merger of bacteremia cases), Haemophilus influenzae (refers only to the β-lactamase-negative strains), or Moraxella catarrhalis bacteria cause persons. · Complicated urinary tract infections, including pyelonephritis: the Escherichia coli or Klebsiella pneumoniae caused by. · Acute pelvic infections, including postpartum endometritis, abortion infection after infection and obstetrics: the Streptococcus agalactiae, Escherichia coli, Bacteroides fragilis, puzzled sugar Porphyromonas bacteria Peptostreptococcus or double Lupuleiwo caused by Escherichia. · Bacteremia.
For the separation and identification of pathogens and determine its susceptibility to ertapenem should be properly taken for bacteriological examination of specimens. In obtaining the results of these checks before you can start using this for empirical treatment; Once inspection results, respond antibiotic regimen adjusted accordingly. In order to reduce the formation of bacterial resistance and to ensure the product's efficacy and other antibacterial drugs, this product can only be used for the treatment or prevention of an identified or highly suspected infections caused by sensitive bacteria. When obtaining bacterial culture and drug susceptibility testing results, should be selected and adjusted accordingly antibiotic treatment. In the absence of the test results before, according to the local epidemiology and susceptibility bacterial characteristics, select the empiric treatment.
More about:Ertapenem Sodium manufacturer
From:Natural herbal extracts
Tuesday, August 6, 2013
Fucus vesiculosus can be used for weight loss
Fucus vesiculosus is a brownish-green atramentous algae that is added frequently accepted as float blow or kelp. It is built-in to the western shores of the Mediterranean Sea and to the North Atlantic coasts. Although it has abounding uses, alignment from ammunition to aliment for cattle, it is aswell a accepted homeopathic remedy. It may be acclimated to anticipate goiter or thyroid disease, to advance weight loss, to amusement rheumatism, and as an antiviral treatment.
This abyssal bulb is both adjustable and strong. Although brownish-green if alive, fucus vesiculosus turns atramentous if it dries out. It has a able odor and an abhorrent taste. This alga contains polysaccharides, polyphenols, and minerals, accurately iodine. The polysaccharides about plan to activate the allowed system, while the iodine works to activate the thyroid.
Many humans affirmation that fucus vesiculosus promotes weight accident through the use of a application or capsules fabricated from the alga. It is believed that back the alga is top in iodine, iodine levels in the physique will access by arresting the capsules or cutting the patch. The physique uses iodine to accomplish the thyroid hormone, which manages the body’s metabolism. Consequently, users achievement there will be an access in the assembly of the thyroid hormone by cutting the application and aswell an access in the body’s metabolism. By accretion the body’s metabolism, a being may be able to lose weight after appliance and dieting.
More about:Fucus vesiculosus suppliers
From:Natural herbal extracts
Monday, August 5, 2013
REPERTAXIN L-LYSINE SALT basic information
CAS Number: 446024-42-6
English name: REPERTAXIN L-LYSINE SALT
English Synonyms: R-(-) -2 - (4-Isobutylphenyl) propionyl MethansulphonaMide L-lysine salt
CBNumber: CB1504464
MF: C20H35N3O5S1
Molecular Weight: 429.57
MOL File: Mol file
REPERTAXIN L-LYSINE SALT Chemical Properties
Storage conditions: 2-8 ° C
Solubility: H2O: 52 mg / mL
form: lyophilized powder
Safety Information
WGK Germany: 3
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From:Natural herbal extracts
Thursday, August 1, 2013
1,3-Benzodioxole-5-ethanamine basic information
CAS: 74341-77-8
English name: 1,3-Benzodioxole-5-ethanamine, alpha-methyl-N-propyl-, hydrochloride
English Synonyms: (±)-N-Propyl-3 ,4-methylenedioxyamphetamine hydrochloride; 1,3-Benzodioxole-5-ethanamine, alpha-methyl-N-propyl-, hydrochloride
CBNumber: CB91238137
MOL File: 74341-77-8.mol
Synonyms: Einecs 245-825-9; RARECHEM AN KA 0317; 7-METHOXY-1 ,3-BENZODIOXO-5-ETHANAMINE; 7-methoxybenzo-1 ,3-dioxole-5-ethylamine; 7-METHOXY-1, 3 - BENZODIOXOLE-5-ETHANAMINE
Molecular formula: C10H13NO3
Molecular weight: 195.22
Product description: This product is light yellow crystal powder and its melting point is 195-198 centidegree. It is mainly used to compound Cefprozil, Cefixime and so on.
More about:13-Benzodioxole-5-ethanamine suppliers
From:Natural herbal extracts
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