Validasi Metode Analisis Dalam Jamu
Daftar pustaka
Chan, C.C.,Lee,Y.C., Lam, H., and Zhang, X.M., 2004, Analytical method validation and instrument performance verification, John Wiley Sons,
Inc., New Jersey, pp. 17,18. Cook, et al., 2000, Pearson’s Product Moment Correlation Coefficient,
http:media3.bmth.ac.ukspssfocus_pagesfocus_10a.htm, diakses
tanggal 16 Agustus 2014 Direktorat Pengawas Obat dan Makanan RI,1974, Farmakope Indonesia, edisi 3,
Departemen Kesehatan Republik Indonesia, Jakarta, pp. 26-30. Direktorat Pengawas Obat dan Makanan RI,1995, Farmakope Indonesia, edisi 4,
Departemen Kesehatan Republik Indonesia, Jakarta, pp. 73-75. Gandjar, I.G
.
dan Rohman,A., 2010, Kimia Farmasi Analisis, Pustaka Pelajar, Yogyakarta, pp.378-400.
Gandjar, I.G
.,
dan Rohman,A., 2012, Analisis Obat Secara Spektrofotometri dan Kromatografi, Pustaka Pelajar, Yogyakarta, pp.417-428.
Gennaro, A.R., Ed., Remington The Science and Practice of Pharmacy, 20
th
ed., Lipincott William and Wilkins, Philadelphia, pp. 1462-1464.
Glaxosmithkline, 2013, Safety Data Sheet of Allopurinol, www.msds-
gsk.comGetSdsFile.ashx?fileId=2421
,
diakses tanggal 1 April 2014 Gonzales, A.G. and Herrador, M.A., 2007, A practical guide to analytical method
validation, Including Measurement Uncertainty and Accuracy Profiles, Trends in Anal. Chem., 26, pp. 232-234.
Harmita, 2006, Analisis Kuantitatif Bahan Baku dan Sediaan Farmasi, Departemen Farmasi FMIPA Universitas Indonesia, Depok, pp. 157-165.
Harvey, D., 2000, Modern Analytical Chemistry, McGraw Hill, New York, pp. 578-586.
Hendayana, S., 2006, Kimia Pemisahan, PT Remaja Rosdakarya, Bandung, pp. 67-112.
Horwitz, W., Latimer, G.W., Eds, 2005, Official Method of Analysis, AOAC International, USA, pp. 254-250.
Iskandar, J.,2006. Rematik dan Asam Urat. Bhuana Ilmu Komputer. Jakarta, pp. 34-38.
Jeffrey, R., 1996, Analytical Detection Limit Guidance Laboratory Guide for Determining Method Detection Limit, Laboratory Certification Program,
Department of Natural Resources, Wisconsin. Jenkins,G.L., 1967, Quantitative Chemical Analysis, Second Edition, W.H.
Freeman and Company, New York Johnstone, A., 2005, Gout The disease and Non Drug Treatment, Hospital
Pharmacist, 12, pp. 391-394 Kantasubrata,J., 2004, Kiat Memahami HPLC, Puslitkimia, LIPI, pp. 12-24.
Kepmenkes RI no 661MENKESSKVII1994, Tentang Persyaratan Obat Tradisional, Departemen Kesehatan RI,Jakarta
Khayoon,W.S, Abaichy,M.Q., Jasim, M., and Hamadany, M.A., 2008, Spectrophotometric Determination of Allopurinol in Tablet Formulation,
Journal of Phisical Science, 192, 23-30. Levin, S., 2002, Quantitative Work in HPLC,
http:forumsci.co.ilHPLC , diakses
tanggal 31 Desember 2013. Long, William dan Henderson, 2007, Chromatography of Nitrogen Containing
Compounds Without Triethylamine, Agilent Technology. Machata, S.G., 2005, Comparison of the OctanolWater Partition Coefficients
Calculated by ClogP
®
, ACDlogP and KowWin
®
to Experimentally Determined Values, International Journal of Pharmaceutics, 294, pp.
185-192. Mayasari, 2009, Analisis Kandungan Metampiron Pada Jamu Tradisional Yang
Beredar Di Kota Medan Tahun 2009, Skripsi, Fakultas Kesehatan Masyarakat, Universitas Sumatra Utara, Sumatra Utara
Mandell and Brian, F., 2008, Clinical manifestation of hyperuricemia and gout, Clinic Journal of Medicine, 153, 256-260.
Medsafe, 2011,
Allopurinol, http:www.medsafe.govt.nzprofsdatasheetaapoallopurinoltab.pdf
, diakses tanggal 1 April 2014
Moffat, C., Osselton, M.D., Widdop, B., 2011, Clarke’s Analysis of Drugs and Poisons, 4
th
edition, Pharmaceutical Press, London, UK, pp. 125-150. Mulja, M., Suharman, 1995, Analisis Instrumental, Airlangga University Press,
Surabaya, pp. 26-27, 33-34. Munson, J.W., 1991, Pharmaceutical Analysis Modern Methods, diterjemahkan
oleh Harjana, Parwa B., Volume II, Airlangga University Press, Surabaya, pp. 12-18.
Mursyidi, A., Volumetri dan Gravimetri, Gadjah Mada University Press, Yogyakarta, pp. 88,89,108.
Permata, D., 2012, Optimasi Metode Identifikasi Antalgin Dan Klorfeniramin Maleat Secara KCKT Photodiode Array Setelah Pemisahan Dengan
Solid Phase Extraction Pada Sediaan Obat Tradisional, Skripsi, Fakultas Matematika Dan Ilmu Pengetahuan Alam Program Ekstensi Departemen
Farmasi, Universitas Indonesia, Depok
Pengawas Obat dan Makanan POM, 2004, Tentang Ketentuan Pokok Pengelompokan dan Penandaan Obat Bahan Alam Indonesia,
Departemen Kesehatan RI, Jakarta. Pengawas Obat dan Makanan POM, 2005, Kriteria dan Tata Laksana
Pendaftaran Obat Tradisional, Obat Herbal Terstandar dan Fitofarmaka, Departemen Kesehatan RI, Jakarta.
Permenkes RI. No. 246MenkesPerV1990, Tentang Izin Usaha Industri Obat Tradisional dan Pendaftaran Obat Tradisional, Departemen Kesehatan
RI, Jakarta. Permenkes RI. No. 007 tahun 2012, Tentang Registrasi Obat Tradisional,
Departemen Kesehatan RI, Jakarta Reinders et al, 2007, A simple method for quantification of allopurinol and
oxypurinol in human by high performance liquid chromatography with uv detection, Journal of Pharmaceutical and Biomedical Analysis, 452,
pp. 312-317.
Sari, M.K., 2014, Optimasi dan Validasi Penetapan Kadar Alopurinol Dalam Matriks Tablet Obat Secara Spektrofotometri UVdan Matriks Sampel
Jamu Asam Urat Secara Kromatografi Cair Kinerja Tinggi, Skripsi, Fakultas Farmasi, Universitas Sanata Dharma, Yogyakarta
Satiadarma, K., 2004, Azas Pengembangan Prosedur Analisis, Edisi pertama, Airlangga University Press, Surabaya, pp. 378-388
Sastrohamidjojo, H., 1991, Kromatografi, Liberty, Yogyakarta, pp. 99-105. Skoog, D.A., West, D.M., Holler, F.J., 1998, Analytical Chemistry, Sixth edition,
Saunders College Publishing, USA, pp. 383-385. Snyder, L.R., Kirkland, J.J., Glajch, J.L., 1997, Practical HPLC Method
Development, 2nd edition, John Wiley Sons, Inc., New York, pp. 25- 28.
Snyder, L.R., Kirkland, J.J., Dolan, J.W., 2010, Introduction of Modern Liquid Chromatography, 3 rd edition, John Wiley Sons, Inc., New York, pp.
25, 28, 33, 40-42, 51-52, 71, 109, 152, 316, 327.