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Cisplatin bioavailability

WebIn attempts to overcome the drawbacks of cisplatin - severe toxicity, drug resistance and poor oral bioavailability - the development of platinum-based drugs has progressed from carboplatin and oxaliplatin to the newest generation of drugs, such as satraplatin, picoplatin and the multinuclear platinum complex BBR3464 (triplatin). WebFeb 28, 2024 · One of the main problems in chemotherapy using platinum drugs as anticancer agents is the resistance phenomenon. Synthesizing and evaluating valid alternative compounds is challenging. This review focuses on the last two years of progress in the studies of platinum (II)- and platinum (IV)-based anticancer complexes. In …

Cisplatin (PIM 132) - International Programme on Chemical Safety

WebFeb 13, 2024 · Bioavailability Describes the rate and concentration at which a drug reaches systemic circulation Expressed as a percentage of the dose that was initially … WebCisplatin is a platinum-based agent whose nephrotoxicity is thought related to the chloride in the cis position. Cisplatin gains entry into tubular cells via uptake by the OCT-2 … solbownone https://beni-plugs.com

Fundamentals of pharmacology - Knowledge @ AMBOSS

WebFeb 1, 2005 · Cisplatin is the first choice treatment in mediastinal germ cell tumors. However, concerns regarding increased toxicity of cisplatin hamper its administration in … WebCorrespondingly, copper depletors are adopted to reduce copper bioavailability, and a variety of copper-based agents, including copper-based nanosystems, copper complexes and nano-copper complexes, are applied to supplement copper. ... Cisplatin is a milestone in the field of metal complexes for cancer treatment, but because of the dose ... WebCisplatin was administered in 10, 14, 18, 22 and 26 mg/kg doses; the control group received saline. Either saline or cisplatin were given three days before the admi … solbrain 46

A better platinum-based anticancer drug yet to come? - PubMed

Category:Cisplatin - an overview ScienceDirect Topics

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Cisplatin bioavailability

(PDF) Synthesis and Characterization of Cisplatin-Loaded

WebNov 21, 2024 · The route of administration will have a direct impact on poor drug bioavailability, especially if administrated via the systemic route due to incomplete absorption or degradation. In conventional drug delivery … WebThe mRNA and protein expression levels of ZO-1 and F-actin began to decrease from the time point of 2 min; the lowest levels in the borneol high-dose (46.7% decrease for ZO-1 and 63.3% for F-actin compared with control) and low-dose groups (54.3% for ZO-1; 77.9% for F-actin) appeared at the time points of 30 and 45 min, respectively.

Cisplatin bioavailability

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WebCisplatin is an antineoplastic agent that is FDA approved for the treatment of metastatic testicular tumors, metastatic ovarian tumors, and advanced bladder cancer. There is a Black Box Warning for this drug as shown here. Common adverse reactions include anemia, leukopenia, and thrombocytopenia . Adult Indications and Dosage WebApproved by the United States Food and Drug Administration (FDA) in 1978, cisplatin has been widely used to treat several types of neoplasms: lung, ovarian, breast, bladder, testicular, and brain cancers, either alone or in combination with other drugs.

WebFeb 1, 2005 · bioavailability, of cisplatin and to evaluate the influence of covariates on the pharmacokinetic variability. Methods: Pharmacokinetic and demographic data were collected from 32 adult patients... WebHyponatremia of grade 3 or above developed in 30.7% of the generic CDDP group compared to 15.1% of the brand-name CDDP group ( P =0.011). Multivariate analysis showed that the use of generic CDDP increased the incidence of hyponatremia (odds ratio =5.661, 95% confidence interval =1.403–22.839; P =0.015). Conclusion: Oncologists …

WebJul 28, 2004 · The oral bioavailability (F) population estimates were, respectively, 0.39 and 0.30 with associated intersubject variabilities (ISV) of 24% and 26%. Peak concentrations following oral dosing occurred at 1.0 h and 1.6 h for … Cisplatin is a platinum based chemotherapy agent used to treat various sarcomas, carcinomas, lymphomas, and germ cell tumors. Brand Names. Platinol. Generic Name. Cisplatin. DrugBank Accession Number. DB00515. Background. Cisplatin, cisplatinum or cis-diamminedichloroplatinum (II) (CDDP) is a … See more

WebJul 7, 2014 · Cisplatin exerts its toxicity by DNA binding and downstream apoptotic signaling, and resistance is conferred by reducing apoptotic signaling, up-regulating DNA …

WebEffect of cisplatin-induced acute renal failure on bioavailability and intestinal secretion of quinolone antibacterial drugs in rats Cisplatin-induced ARF differentially modulated the bioavailability and intestinal secretion of quinolones in rats. solbrain archiveWebCisplatin, one of the most active cytotoxic agents against cancer, has several toxicities. Hepatotoxicity is one of them occurred during high doses treatment. The aim of this study was to determine the effects of erdosteine against cisplatin-induced liver injury through tissue oxidant/antioxidant parameters and light microscopic evaluation. slytherin tumblerWebApr 11, 2024 · Cisplatin (CISPt) III: Systemic: Lipid coated ... The bioavailability was calculated according to the Area Under the Curve (AUC) values, and the ABZ availability when administered orally ABZ-NCs was similar to [email protected] (531.16 ± 136.11%, and 476.35 ± 87.11% respectively). In conclusion, the NCs-MAPs combination achieved a … solbrenthetWebJan 1, 1985 · Cisplatin is generally synthesised by the ammonolysis of potassium tetrachloroplatinate (K 2 PtC1 4 ). The absorption spectrum of cisplatin (1.0 mg/ml) has been obtained in 0.1 N HCl using a Cary 15 and 2.0 cm cells.The spectrum shows three maxima at 203 nm, 301 nm, and 362 nm, a “shoulder” at 285 nm, and minima at 246 nm … solbrew company in solomon islandsWebCisplatin Injection is indicated as a single agent for patients with transitional cell bladder cancer which is no longer amenable to local treatments, such as surgery and/or r … solbrew company ltdWebFeb 16, 2024 · 50 to 70 mg/m2 by slow IV infusion once every 3 to 4 weeks; for heavily pretreated patients, an initial dose of 50 mg/m2 by slow IV infusion once every 4 weeks … sol breathworkWebMay 13, 2024 · To improve the bioavailability and tolerance of drugs, recent advances in nanotechnology promote the development of nanoparticle-based drug delivery systems, which is widely used in cancer chemotherapy (Lepeltier et al., 2024; Su et al., 2024). Nanoparticles have advantages including good biocompatibility, low toxicity, long … solbrew products