| Effect of Zinc Sulfate in Protection against Cisplatin-Induced Nephrotoxicity in Cancer Patients | |
| بحث |
النوع: |
| صيدلة |
التخصص العام: |
| Abbas M. Al-sarraf |
اسم الناشر: |
| Arif S. Malik2, Hayder B. Sahib*3, Adeeb A. Al-zubaidy3, Haider N. Salih4, Imad K. Alwan5, Ayad A. Hussein1 |
اسماء المساعدين: |
| International Journal of Pharmaceutical Sciences Review and Research |
الجهة الناشرة: |
| International Journal of Pharmaceutical Sciences Review and Research (Int J Pharm Sci Rev Res) is an open access, bi-monthly published, peer-reviewed, international online journal.
The journal will cover topics related to Pharmaceutical Sciences (Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Novel Drug Delivery, Pharmaceutical/Medicinal Chemistry, formulation technology, pharmaceutical product development, nutraceutical product development, cosmetic product development, Pharmacognosy and Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest, quality assurance, herbal technology, regulatory affairs, Pharmaceutical marketing, Biological sciences, Botany, Zoology, Biochemistry etc.).
Index copernicus value: 5.19 (ICV 2011: 5.19)
Our International Journal of Pharmaceutical Sciences Review and Research (IJPSRR) achieved a good index copernicus value in short span of time amongst International community with great impact.
Calculated 3 years Impact factor (as of 31st December 2015) = 2.544
Elsevier's SCImago Impact factor = 0.65 |
|
| 2014 |
سنة النشر: |
الخلاصة
Cisplatin is a potent antitumor agent that is useful in chemotherapy of various types of cancers. Currently, nephrotoxicity limits its
usefulness. The main mechanism responsible for nephrotoxicity is oxidative stress with associated inflammation. This study was to
evaluate the protective effect of zinc sulphate on cisplatin-induced nephrotoxicity in cancer patients. Twenty eight patients were
participated in the study and were randomized into two groups. Patients in group I (N=14) received six cycles of cisplatin based
regimen every 21 days. Patients in group II (N=14) received zinc sulphate in addition to cisplatin based regimen. Serum cystatin C
and cystatin C-based GFR were measured at base line and 21 days after 1, 2, 4 and 6 cycles while urinary malondialdehyde and IL-18
were measured at base line and 1 day after 1, 2, 4 and 6 cycles of cisplatin based regimen. Zinc sulfate addition to cisplatin in group
II significantly (P<0.05) ameliorated the cisplatin-induced increment in serum cystatin C, urinary malondialdehyde and IL-18 and the
cisplatin-induced decline in cystatin C-based GFR that were demonstrated in group I. The significant protective effect of zinc sulfate
on cisplatin-induced nephrotoxicity may be through its antioxidant and anti-inflammatory action. |
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