enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Antimicrobial pharmacodynamics - Wikipedia

    en.wikipedia.org/wiki/Antimicrobial_pharmacodynamics

    Therefore, an antibiotic with PAE would require less frequent administration and it could improve patient adherence with regard to pharmacotherapy. [ 3 ] [ 5 ] Proposed mechanisms include (1) slow recovery after reversible nonlethal damage to cell structures; (2) persistence of the drug at a binding site or within the periplasmic space ; and (3 ...

  3. Glycopeptide antibiotic - Wikipedia

    en.wikipedia.org/wiki/Glycopeptide_antibiotic

    Glycopeptide antibiotics are a class of drugs of microbial origin that are composed of glycosylated cyclic or polycyclic nonribosomal peptides.Significant glycopeptide antibiotics include the anti-infective antibiotics vancomycin, teicoplanin, telavancin, ramoplanin, avoparcin and decaplanin, corbomycin, complestatin and the antitumor antibiotic bleomycin.

  4. Category:Pharmacokinetics templates - Wikipedia

    en.wikipedia.org/wiki/Category:Pharmacokinetics...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  5. Distribution (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Distribution_(pharmacology)

    Distribution in pharmacology is a branch of pharmacokinetics which describes the reversible transfer of a drug from one location to another within the body.. Once a drug enters into systemic circulation by absorption or direct administration, it must be distributed into interstitial and intracellular fluids.

  6. Area under the curve (pharmacokinetics) - Wikipedia

    en.wikipedia.org/wiki/Area_under_the_curve...

    The use of trapezoidal rule in AUC calculation was known in literature by no later than 1975, in J.G. Wagner's Fundamentals of Clinical Pharmacokinetics. A 1977 article compares the "classical" trapezoidal method to a number of methods that take into account the typical shape of the concentration plot, caused by first-order kinetics. [8]

  7. Staurosporine - Wikipedia

    en.wikipedia.org/wiki/Staurosporine

    Staurosporine (antibiotic AM-2282 or STS) is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus. [1] It was the first of over 50 alkaloids that were discovered to share this type of bis-indole chemical structure. The chemical structure of staurosporine was elucidated by X-ray crystalography in 1994. [2]

  8. Template:Pharmacokinetics of long-acting injectable ...

    en.wikipedia.org/wiki/Template:Pharmacokinetics...

    Pharmacokinetics of long-acting injectable antipsychotics; Medication Brand name Class Vehicle Dosage T max t 1/2 single t 1/2 multiple logP c Ref Aripiprazole lauroxil: Aristada: Atypical: Water a: 441–1064 mg/4–8 weeks: 24–35 days? 54–57 days: 7.9–10.0: Aripiprazole monohydrate: Abilify Maintena: Atypical: Water a: 300–400 mg/4 ...

  9. Ceftolozane/tazobactam - Wikipedia

    en.wikipedia.org/wiki/Ceftolozane/tazobactam

    [6] [5] [7] Ceftolozane is a cephalosporin antibiotic, developed for the treatment of infections with gram-negative bacteria that are resistant to conventional antibiotics. [8] It was studied for urinary tract infections, intra-abdominal infections and ventilator-associated bacterial pneumonia.