Keywords: شیمی درمانی سرطان; clinical pharmacokinetics; pediatric; pharmacokinetic/pharmacodynamic models; population pharmacokinetics; cancer chemotherapy;
مقالات ISI شیمی درمانی سرطان (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: شیمی درمانی سرطان; Optimal control; Switched systems; Binary functions; Drug therapy; Cancer chemotherapy;
Keywords: شیمی درمانی سرطان; prodrugs; cancer chemotherapy; targeted drug delivery; peptide delivery; polymeric drugs;
Keywords: شیمی درمانی سرطان; Drug delivery systems; Cancer chemotherapy; Drug targeting; Image analysis; Flow chamber;
Keywords: شیمی درمانی سرطان; Microparticles; Drug delivery system; Yeast; Doxorubicin; Macrophages; Cancer chemotherapy;
Keywords: شیمی درمانی سرطان; Polydopamine nanoparticles; Surface modification; Hydroxyethyl starch; Cancer chemotherapy;
Keywords: شیمی درمانی سرطان; Cancer chemotherapy; Informed consent; Palliative care; Prognosis communication; Video intervention; Patient-centered communication;
Keywords: شیمی درمانی سرطان; Liposome; Nanoparticle; Paclitaxel; Hydrophobic drug; Drug delivery; Cancer chemotherapy;
Keywords: شیمی درمانی سرطان; Cancer chemotherapy; Cognition dysfunction; Chemobrain; Cytokines and epigenetics changes;
Keywords: شیمی درمانی سرطان; Cardiotoxicity; Cancer chemotherapy; Cardiac function; Terminalia; Echocardiography; Cardioprotection; CO; cardiac output; DHE; dihydroethidin; DOX; doxorubicin; EF; ejection fraction; FS; fractional shortening; JC-1; 5,5â²,6,6â²-tetrachloro-1,1â²,3,3â
Keywords: شیمی درمانی سرطان; Cancer chemotherapy; Magnetic resonance imaging; Magnetic nanoparticles; Targeted drug delivery;
Keywords: شیمی درمانی سرطان; Aprepitant; Cancer chemotherapy; Solubility; Empirical models; Equation of state (EoS); Modeling;
Keywords: شیمی درمانی سرطان; cisplatin; nephrotoxicity; population pharmacokinetics/pharmacodynamics; pharmacokinetic/pharmacodynamic models; toxicokinetics; simulations; cancer chemotherapy;
Keywords: شیمی درمانی سرطان; cancer chemotherapy; polymeric drug delivery systems; controlled release; pharmacokinetics; synthesis; biodegradable polymers;
Keywords: شیمی درمانی سرطان; mPEG–PGA; Doxorubicin hydrochloride; Nanorods; Electrostatic interaction; Cancer chemotherapy
Keywords: شیمی درمانی سرطان; thermosensitive; paclitaxel liposome; intratumoral retention; pharmacodynamics; tissue distribution; biodegradable polymers; cancer chemotherapy; controlled release; injectables; lymphatic transport; thermal gels;
Keywords: شیمی درمانی سرطان; nanotechnology; nanoparticles; cancer; biomaterials; cancer chemotherapy; drug resistance;
Keywords: شیمی درمانی سرطان; Biosurfactants; Cancer chemotherapy; Critical micelle concentration; Cytotoxicity; HEK 293; MCF-7; Rhamnolipid; Sophorolipid; Surfactin; THP-1;
Keywords: شیمی درمانی سرطان; Measurement-based cancer control; Cancer chemotherapy; Killing cancerous cells; PID controller design; Frequency response data
Keywords: شیمی درمانی سرطان; Cisplatin delivery; Cancer chemotherapy; Nanoparticle; Electrohydrodynamic atomization; Controlled release;
Keywords: شیمی درمانی سرطان; cancer chemotherapy; pharmacodynamics; drug effects; efflux pumps; cell lines;
Keywords: شیمی درمانی سرطان; pharmacokinetic/pharmacodynamic models; simulation; drug interaction; cancer chemotherapy; in silico modeling;
Keywords: شیمی درمانی سرطان; hydromorphone; ketamine; drug delivery; microparticles; intrathecal; pharmacodynamics; poly(lactic-co-glycolicacid)(PLGA); rat model of chemotherapy-induced peripheral neuropathy (CIPN rats); cancer chemotherapy; intractable cancer-related pain;
Keywords: شیمی درمانی سرطان; caffeic acid phenethyl ester; nanoparticles; metastasis; invasion; cancer chemotherapy; natural products; polymeric drug carrier;
Keywords: شیمی درمانی سرطان; biophysical models; cancer chemotherapy; controlled release; dissolution; drug delivery systems; in vitro models; liposomes; nanoparticles; permeability; transport;
Keywords: شیمی درمانی سرطان; Cancer chemotherapy; Model uncertainty; Lyapunov stability; Adaptive control; Robust performance;
Keywords: شیمی درمانی سرطان; lapatinib; paclitaxel; poorly water-soluble drugs; solubility; micelle; cancer chemotherapy; sensitize; human epidermal growth factor receptor-2; polymeric drug delivery systems; conjugation;
Keywords: شیمی درمانی سرطان; Release kinetics; Liposomes; DOXIL; Dynamic dialysis; Mechanistic modeling; Cancer chemotherapy;
Keywords: شیمی درمانی سرطان; intravesical instillation; drug delivery systems; controlled release; biodegradable polymers; thermal gels; cancer chemotherapy; ADR Adriamycin; HSA human serum albumin; NP-ADR Adriamycin-loaded HSA nanoparticles; NP-ADR-Gel NP-ADR-loaded hydrogel; TCC tr
Keywords: شیمی درمانی سرطان; diadduct malonic acidâfullerene; micelles; photosensitive; excipients; cellular mechanisms; pharmacokinetics; cancer chemotherapy; controlled release/delivery; antitumor effect;
Keywords: شیمی درمانی سرطان; Cancer stem-like/tumor-initiating cells; Cell biomechanics; Atomic force microscope; Cancer chemotherapy; Cellular differentiation;
Keywords: شیمی درمانی سرطان; ADME; clinical pharmacokinetics; drug interactions; membrane transporter; drug metabolizing enzymes; cancer chemotherapy;
Keywords: شیمی درمانی سرطان; Conjugates; Fatty acids; Microtubule-binding drugs; Cancer chemotherapy; Drug resistance reversal;
Keywords: شیمی درمانی سرطان; controlled release; drug delivery systems; formulation; injectables; cancer chemotherapy; phospholipids;
Keywords: شیمی درمانی سرطان; Cancer chemotherapy; Parametric uncertainty; Robust control; Optimal control; Linear regulation; Variation of extremals;
Metabolic Pathway of Icotinib In Vitro: The Differential Roles of CYP3A4, CYP3A5, and CYP1A2 on Potential Pharmacokinetic Drug-Drug Interaction
Keywords: شیمی درمانی سرطان; drug interaction; drug metabolizing enzyme; cancer chemotherapy; human liver microsomes; in vitro-in vivo correlations (IVIVC); mass spectrometry; CYP; cytochrome P450; HRMS; high-resolution mass spectrometer; LC; liquid chromatography; MS; mass spect
Chitosan-grafted-poly(methacrylic acid)/graphene oxide nanocomposite as a pH-responsive de novo cancer chemotherapy nanosystem
Keywords: شیمی درمانی سرطان; Chitosan; Poly(methacrylic acid); pH-responsive; Graphene oxide; Drug delivery; Cancer chemotherapy;
Synthesis, DNA binding and cytotoxic activity of pyrimido[4â²,5â²:4,5]thieno(2,3-b)quinoline with 9-hydroxy-4-(3-diethylaminopropylamino) and 8-methoxy-4-(3-diethylaminopropylamino) substitutions
Keywords: شیمی درمانی سرطان; DNA intercalators; Anticancer; DNA; Cancer chemotherapy; PTQ;
Antineoplastic activity of mitomycin C formulated in nanoemulsions-based essential oils on HeLa cervical cancer cells
Keywords: شیمی درمانی سرطان; Cell culture; Cancer chemotherapy; Colloid; Nephelometry; Light-scattering; Fluorescence spectroscopy; MMC; mitomycin C; ESSO; essential oil; Ch; chamomile; Gar; Garlic; NE; nanoemulsion; Ch-NE; chamomile-loaded NE; Ch-MMC; MMC-loaded NE-based chamomile o
A polyethyleneimine-driven self-assembled nanoplatform for fluorescence and MR dual-mode imaging guided cancer chemotherapy
Keywords: شیمی درمانی سرطان; Self-assembled nanocluster; Lanthanide-doped CaF2; pH triggered cisplatin release; Fluorescence/MR imaging; Cancer chemotherapy;
Anthracycline-induced cardiotoxicity: A multicenter randomised trial comparing two strategies for guiding prevention with enalapril: The International CardioOncology Society-one trial
Keywords: شیمی درمانی سرطان; Anthracyclines; Troponin; Cancer chemotherapy; Clinical trial; Cardiotoxicity; Enalapril;
Therapeutic efficacy of rebamipide-loaded PLGA nanoparticles coated with chitosan in a mouse model for oral mucositis induced by cancer chemotherapy
Keywords: شیمی درمانی سرطان; Rebamipide; Oral mucositis; Nanoparticle; Poly(dl-lactide-co-glycolide); PLGA; Chitosan; Therapeutic efficacy; Mucin: mouse; Cancer chemotherapy;
The mechanism of tumour cell death by metal-based anticancer drugs is not only a matter of DNA interactions
Keywords: شیمی درمانی سرطان; 15-LOX-1; 15-lipoxygenase; AIF; apoptosis inducing factor; APC; adenomatous polyposis coli; AKT or PKB; protein kinase B; ATG16L2; autophagy related 16 like 2; AUC; area under the curve; Bad; Bcl-2 associated death promoter; Bcl-2; B-cell lymphoma 2; Bcl-
Indications for Postmastectomy Radiation After Neoadjuvant Chemotherapy in ypN0 and ypN1-3 Axillary Node-Positive Women
Keywords: شیمی درمانی سرطان; Cancer chemotherapy; Mastectomy; Neoadjuvant chemotherapy; Postmastectomy radiation; Radiation therapy;
NCS-1 is a regulator of calcium signaling in health and disease
Keywords: شیمی درمانی سرطان; Calcium signaling; Calcium binding proteins; Paclitaxel; Cancer chemotherapy; Peripheral neuropathy; CIPN;
Suitability of the AUC Ratio as an Indicator of the Pharmacokinetic Advantage in HIPEC
Keywords: شیمی درمانی سرطان; Clinical pharmacokinetics; Simulations; Cancer chemotherapy; Absorption; Mathematical models; Clearance; HIPEC; hyperthermic intraoperative peritoneal chemotherapy; iv; intravenous; PKA; pharmacokinetic advantage; ka; absorption rate constant; ka_app; app
Synthesis, characterization and interactions with 9-methylguanine of ruthenium(II) η6-arene complexes with aromatic diimines
Keywords: شیمی درمانی سرطان; η6-Arene ruthenium; 9-Methylguanine; Cancer chemotherapy; NMR; Mass spectrometry;
5-Fluororacil-Induced Gastrointestinal Damage Impairs the Absorption and Anticoagulant Effects of Dabigatran Etexilate
Keywords: شیمی درمانی سرطان; bioavailability; cancer chemotherapy; gastrointestinal; intestinal absorption; P-glycoprotein; pharmacokinetics/pharmacodynamics;
Dehydroascorbic Acid and pGPMA Dual Modified pH-Sensitive Polymeric Micelles for Target Treatment of Liver Cancer
Keywords: شیمی درمانی سرطان; drug delivery systems; polymeric drug delivery systems; cancer chemotherapy; biodegradable polymers; biomaterials; controlled release;
Development and in-vitro characterization of nanoemulsions loaded with paclitaxel/γ-tocotrienol lipid conjugates
Keywords: شیمی درمانی سرطان; Nanoemulsion; Paclitaxel; Tocotrienol; PEGylation; Vitamin E TPGS; Drug delivery; Cancer chemotherapy; Nanotechnology;