DAFTAR PUSTAKA

Agilent Technologies., 2009. Fundamentals of Gas Chromatography.

AHFS, 2016. AHFS Drug Information. American Society of Health Sistem

Pharmacist, Wisconsin, USA.

Aiache, J.M. 1993. Farmasetika 2 Biofarmasi. Edisi ke-2. Penerjemah: Dr. Widji
Soeratri. Surabaya: Penerbit Airlangga University Press. Hal. 7.

Altaher, A.Y. 2005. Pharmacokinetics Of Diclofenac In Sheep Following Intra

Venous and Intramuscular Administration. Saudi Pharmaceutical Journal.
Vol 13, No.2-3. Pages 107-108.
Anderson, P.O., Knoben, J.E., and Troutman, W.G. 2002. Handbook of Clinical
Drug Data (10th edition). USA: McGRAW-HILL Medical Publishing
Division.

Arcelloni, C, et al., 2001. High Performance Liquid Chromatography

Determination of Diclofenak in Human Plasma after Solid-Phase extraction.
Journal of Chromatography B. 763. 195-200.

Badan Pengawas Obat dan Makanan. 2004. Pedoman Uji Bioekivalensi. Dalam:
Peraturan Kepala Badan Pengawas dan Makanan Republik Indonesia Nomor:
HK.00.05.3.1818. Jakarta.

Badan Pengawas Obat dan Makanan. 2011. Peraturan Badan Pengawas Obat dan
Makanan RI No. Hk. 03. 1. 23. 12. 11. 10217 tahun 2011 Tentang Obat Wajib
Uji BE. Jakarta
Baghel, U.S, et al., 2010. Review Article on Ultra Performance Liquid
Chromatography (UPLC); A Chromatography Technique. International
Journal of Pharmaceutical Quality Assurance. 19-20.

Basmenji. S, Hadi Valizadeh and Parvin Zakeri-Milani. 2011. Comparative In Vitro

Dissolution and In Vivo Bioequivalence of Two Diclofenac Enteric Coated
Formulations, Arzneimittelforschungg, vol.61(10), 566-570.

Emami. J, Ghassami N and Talari R. 2007. A Rapid and Sensitive Modified HPLC
Method for Determination of Diclofenac in Human Plasma and Its
Application in Pharmacokinetic Studies. DARU. Vol 15(3), 132-138.

EMEA. 2011. Committee for Medicinal Products for Human Use (CHMP)
“Guideline on Bioanalytical Method Validation”,
EMEA/CHMP/EWP/192217/2009 Rev.1 Corr.

Farmakope Indonesia. 2014. Kementrian Kesehatan Republik Indonesia, Edisi V,

hlm. 330-331.

37
Fuad, M.F., 2012. Pengembangan Metode Analisis Dextromethorphan HBr dan
Diphenhydramin HCl dalam Sediaan Obat Batuk Cair Menggunakan Ultra
Performance Liquid Chromatography (UPLC). Skripsi. Universitas Pakuan
Bogor. hal. 1-2.

Goodman dan Gilman’s. 2012. Dasar Farmakologi Terapi. Diterjemahkan oleh

Tim Ahli Bahasa Sekolah Farmasi ITB. Edisi 10. EGC, Jakarta. Hal.578.

Guillarme, D. and Veuthey, J.L., 2011. Guidelines for the Use of UHPLC
Instruments: Requirements for UHPLC Instruments, Method Development in
UHPLC and Method Transfer From Regular HPLC to UHPLC. Laboratory
of Analytical Pharmaceutical Chemistry, University of Geneva. p. 1.

Hill, E., 2014. The Case for Upgrading Existing HPLC Assays to UPLC. Article In:
http://www.impactanalytical.com/Userfiles/Whitepapers/UPLC-Assay-
Whitepaper.pdf, diakses pada 20 Februari 2018.

Hinz, B. 2005. Bioavailability of Diclofenac Pottassium at Low Doses. Germany:

Department of Experimental and Clinical Pharmacology and Toxicology,
Friedrich Alexander University Erlangen-Nurnberg, Fahrstrasse 17, D91054
Erlangen. Pages 80-81.
Katzung Betram G., Masters Susan B., Trevor Anthony J. 2012. Farmakologi
Dasar dan Klinik. Terjemahan: Pendit Brahm U, Soeharsono Ricky. EGC,
Jakarta. Hlm. 697-713.

Kusumaningtyas, A.N., 2016. Optimasi dan Validasi Metode Analisis Atovastatin

dalam Plasma In Vitro secara Kromatografi Kinerja Ultra Tinggi-Tandem
Spektrofotometer Massa (KCKUT-SM). Skripsi. Universitas Muhammadiyah
Prof. Dr. Hamka. Hal 4.

Martindale, 1996. The Complete Drug Reference. London: The Pharmaceutical

Press.

Mohammed. F.A, S.S Alsokari, M.E Wagih, N.M Abdel-Hamid, and S.M Saad-
Eidin. 2014. New HPLC Method for Determination of Diclofenac Sodium in
Human Plasma and its Apllication to Pharmacekinetics Studies After Oral
Administration of Voltaren 50 Mg Tablets to Twelve Healthy Volunteers, Int
J Innovations Sci Pharm. vol.3, 51-62.
Mycek, Mary J, Richard A. Harvey, and Pamela C. Champe. 2001. Farmakologi
Ulasan Bergambar Edisi 2. Jakarta: Widya Medika.

Nasir, F, et al., 2011. Simultaneous Determination of Timolol Maleate,

Resuvastatin Calcium and Diclofenac Sodium in Pharmaceuticals and
Physological Fluids usig HPLC-UV. Journal of Chromatography B. 3434-
3443.

Neal, M.J. 2006. At A Glance Farmakologi Medis. Edisi Kelima. Surabaya:

Penerbit Erlangga. Hal. 32-33.

38
Rôskar, Robert, Vojko Kmetec. 2003. Liquid Chromatographic Determination of
Diclofenac in Human Sinovial Fluid. J. Chromatogr. 788: 57-64.

Shargel, L. dan Yu. 2005. Biofarmasetika dan Farmakokinetika Terapan. Edisi

Kedua. Surabaya: Airlangga University Press. Hal. 449-453.
Siswandono dan Soekardjo, B. 2000. Kimia Medisinal Edisi 2 halaman 228-232,
234, 239. Surabaya: Airlangga University Press.
Skoog, Douglas A, Leary, James J. 1992. Principle of Instrumental Analysis 4th
edition. Florida: Saunders College Publishing. hal 628-667.
Stoelting, R.K., and Hillier, S.C., 2006. Local Anesthetics in Handbook of
Pharmacology and Physiology in Anesthetic Practice, 2nd Edition.
Philadelphia : Lippincott Wiliams & Wilkins. Halaman : 179-207.
Sunil, K. R, G. Balammal, and A. Saravana Kumar. 2012. Ultra Performance Liquid
Chromatography and Review. International Journal of Pharmaceutical
Research and Analysis. Vol 2. 24-31.

Tan Hoan dan Kirana Rahardja. 2007. Obat-obat Penting Khasiat, Penggunaan dan
Efek-efek Sampingnya Edisi Keenam. Jakarta: Elex Media Komputindo.

Yilmaz. B, Ali Asci, and Saziye Sezin Palabiyik. 2011. HPLC Method for
determination of diclofenac in human plasma and its application to
pharmokinetic study in Turkey. Journal of Chromatographic Science. Vol 49.

39