DAFTAR PUSTAKA

Agoes, G. 2012, Sediaan Farmasi Padat (SFI-6). Penerbit ITB, Bandung.

Amstrong, N.A. 2006, Pharmaceutical Experimental Design and Interpretation,

2nd edition, Taylor& Francis Group, New York, pp 118-119.

Ansel, H.C., Allen, L.V. & Popovich, N.G. 1999, Pharmaceutical Dosage Form
and Drug Delivery System, 7th edition, Lippincott Williams & Wilkins a
Wolters Kluwer Company, Philladelphia, pp 229-243.

Ballard, E.B. 1978, An Overview of Prolonged Action Drug Dosage Form, in

Robinson, J.R. (Ed), Sustained and Controlled Release Drug Delivery
Systems, 6 14, Marcel Dekker, New York.

Baumgartner, S., Kristel, J., Vreer, F., Vodovipec, P. & Zorko, B. 2000,
Optimization of Floating Matrix Tablet and Evaluation of their Gastric
Residence Time, Int. J.Pharm, 195: 125-135.

Bhardwaj, T.R., Kanwar, M., Lal, R., dan Gupta, A. 2000, Natural Gums and
Modified Gums as Sustained Release Carriers, Drug Dev. Ind. Pharm.,
26(10):1025-1038.

Cahyani, I.M. 2012, Optimasi Formula Tablet Floating Gastriretentive Nifedipin

menggunakan Metode Effervescent dengan Matriks K100M dan
Etilselulosa, Tesis, Yogyakarta, UGM Yogyakarta.

Chandira, M., Bhovesh, B.S. Venkateswarlu, B. Jayakar, D. Bhowmik, Chiranjib

& K.P. Sampath Kumar, 2009, Studies on Formulation and Evaluation of
Floating Tablets Containing Anti-Ulcer Drugs, Scholars Research
Library Der Pharmacia Letere, 1(2):102-114.

Collett, J. & Moreton, C. 2002, Modified-release Peroral Dosage Form, dalam

Aulton, M.E., Pharmaceutics: the Science of Dosage Form Design, 2nd
edition, Churchill Livingstone, New York, pp 289-305.

Colombo, P., Santi, P., Bettini, R., Brazel, C.S., and Peppas, N.A. 2000, Drug
Release from Swelling Controlled Systems, dalam Wise, D.L.,
Handbook of Pharmaceutical Controlled Release Technology, 183 205,
Marcel Dekker Inc., New York.

Costa, P. & Lobo, J.M.S. 2001, Modelling and Comparison of Dissolution

Profiles, EJPS 13 (2001) 123-133.

78
Daniel, W.W. 2000, Analysis of variance. Biostatistic: A Foundation for Analysis
in the Helth Science, 7th edition, John Wiley & Sons, New York, pp 126-
141.

Dehghan, M.H.G. & Khan, F.N. 2009, Gastroretentive Drug Delivery System: A
Patent Perspective, Int. J. Health Res,2(1):23-24.

Departemen Kesehatan Republik Indonesia, 1979, Farmakope Indonesia, Edisi

III, Jakarta.

Departemen Kesehatan Republik Indonesia, 1995, Farmakope Indonesia, Edisi

IV, Jakarta.

Fudholi, A. 2013, Disolusi & Pelepasan Obat in-vitro, Pustaka Pelajar.

Yogyakarta.

Gandjar, I.G. & Rohman, A. 2007, Kimia Farmasi Analisis, Pustaka Pelajar,
Yogyakarta.

Ghosh, S., Gosh N.S., Debnath, S., Kumar, G.G., Chakraborty, R. & Sen, S. 2010,
Sustain Release Dosage Form of Nifedipine Hydrochloride using Multi-
Unit Chitosan Treated Alginate, IJPBR, 1(4):124-131.

Hardjono, S. 2000, Hubungan Struktur-aktivitas Obat Kardiovaskular, dalam

Siswandono & Soekardjo, B. 2008, Kimia Medicinal, Airlangga
Universy Press, Surabaya.

Helrich, K. (ed). 1990, Official Methods of Analysis of The Association of Official

Analitical Chemists (15th edn). AOAC Inc. Arlington.

Jantzen, G.M. & Robinson, J.R. 1996, Sustained and Controlled Release Drug
Delivery Systems, dalam Banker, G.S., Rhodes, C.T. (eds), Modern
Pharmaceutics, Ed. III, 575 609, Marcel Dekker Inc., New York.

Kavitha, K., Sudir K.Y. & Tamizh, M.T. 2010, The Need Floating Drug Delivery
System: A Review, RJPBCS, 1(2):396 405.

Lachman, L., Lieberman, H. A. & Kanig, J.L. 2008, Teori dan Praktek Farmasi
Industri edisi 3 Jilid 2, diterjemahkan dari bahasa Inggris oleh Suyatmi,
S. Universitas Indonesia Press, Jakarta, 685.

Lende, P.K., M.S. Junagade & Arundati, D.D. 2012, Formulation Optimization
and In-vitro Evaluation of Floating Tablet of Stavudin, Am. J.
PharmTechRes., 2(5):723-739.

79
Lowman, A., and Peppas, N.A. 1999, Hydrogels, Ensyclopedia of Controlled
Drug Delivery, Vol I, 405, A Wiley Interscience Publication, Canada

Martin, A., Swarbick, J. dan Cammarata, A. 1993, Physical Pharmacy, Physical

Chemical Principles in The Pharmaceutical Sciences, Lea & Febiger,
USA.

Modi, V.S., Yogesh, S.T. & Shashikant, C.D. 2010, Formulation and Evaluation
of Controlled Release Delivery of Tramadol Hydrochlorida Using 32
Full Factorial Design, IJCRGG, 2(1):669-675.

Moffat, A.C., Osselton, M.D. & Widdop, B. 2011, Clarkes Analysis of Drugs and
Poisons.4th Ed., Pharmaceutical Press, London, 1777-1778.

Musnina, W.O.S. 2012, Optimasi Formula Tablet Nifedipin Gelling Floating-

Gastroretentive Menggunakan Matriks HPMC K4M, Carbopol 940 dan
Eudragit RSPO, Tesis, Yogyakarta: UGM Yogyakarta.

Nurjayanti, I. 2008, Optimasi Formula Tablet Lepas Lambat Nifedipin dengan

Sistem Matrik Hidroksipropil Metilselulosa, Etil Selulosa dan Laktosa,
Tesis, Universitas Gadjah Mada, Yogyakarta.

Paradkar, A. & Bakliwal,S. 2008, Biopharmaceutics and Pharmacokinetics, Nirali

Prakashan, Pune, India.

Radhakrishna, M., K.G. Parthiban, Nelluri, R., Nagapuri, S.D. & Perumulla A.
2012, Formulation and Evaluation of Floating Drug Delivery System of
Amoxycillin Trihydrate, IRJP,3(8):233-237.

Rao, Y.M., Veni, J.K. & Jayasagar, G., 2001, Formulation and Evaluation of
Diclofenac Sodium Using Hydrophilic Matrices, Drug Dev. Ind. Pharm.,
27(10):759-766.

Rocca, J.G., Omidin, H. & Shah, K. 2003, Progresses in Gastro Drug Delivery
Systems, Business Briefing pharmatech, 15(3):152-156.

Rowe, C.R., Sheske, P. & Quinn, M.E. 2009, Handbook of Pharmaceutical

Excipient, 6th edition, Pharmaceutical Press and American Pharmacist
Association, London and Chicago.

Shah, S.H., Patel, J.K. & Patel, N.V. 2009, Stomach Specific Floating Drug
Delivery System: A Review, Int J.PharmTech., 3:623-633.

Shaikh, K.N.,Payghan, S.A. & Desouza, J.I. 2011, Formulation of Gastroretentive

Drug Delivery System (Floating Tablets) of Nifedipine, IJPBS, 1(2):1-8

80
Shargel, L., Pong, S.W. & Yu, A. 2004, Applied Biopharmaceutics &
Pharmacokinetics, Mc Graw Hill Education, USA.

Shim, S.C., Pae, A.N. & Lee, Y.J. 1988, Mechanistic Study on the Photochemical
Degradation of Nifedipine, Bulletin of The Korean Society, 9(5):1-4.

Shojael, A.H. 2006, Gastric Retentive Dosage Forms. in Li, X. & Jasti, B.R.
(ed). Design of Controlled Release Drug Delivery System.The McGraw-
Hill Companies.Inc. New York, 1-5.

Singh, L.P., Rajesh, K.S., Umalkar, D.G., Chauhan, V.K., Rana, V. & Vasava,
K.S. 2011, Floating Effervescent Tablet : A Review, J. Pharm and Bio.
Sci. 5(5):1-6.

Sinko, P.J. & Singh, H. (ed). 2011, Martins Physical Pharmacy and
Pharmaceutical Sciences Physical Chemical and Biopharmaceutical
Principles in the Pharmaceutical Sciences, 6th Ed., Lippincott
Williams&Wilkins a Wolters Kluwer Business, Philadelphia, 300-317.

Siregar, C.J.P. & Wikarsa, S. 2010, Teknologi Farmasi Sediaan Tablet Dasar-
Dasar Praktis, Buku Kedokteran EGC, Jakarta.

Siswanto, A. & Sulihtyowati, S. 2006, Optimasi Formulasi Sediaan Tablet Lepas

Lambat Teofilin dengan Bahan Matrik HPMC, Na CMC dan Xanthan
Gum, MFI. 17(3):143-148.

Sreekanth, S.K., Palanichany, S., Sekharan, T.R., Thirapathi, A. & Thanga, 2010,
Formulaion and Evaluation Studies of Floating Matriks Tablet of
Nifedipin, IJPBS, 1(2):1-8.

Sugiyono, 1999, Statistika Untuk Penelitian Penelitian, Cetakan ke-2, CV

Alfabeta, Bandung.

Sweetman, S.C. 2009, Martindale The Complete Drug Reference, Vol. I, 36th Ed.,
Pharmaceutical Press, London.

The United States Pharmacopeial Convention Inc, 2007, The United States
Pharmacopeia, 30rd Edition, Rockville.

Voigt, R. 1994, Buku Pelajaran Teknologi Farmasi. Edisi Kelima, diterjemahkan

dari bahasa Inggris Oleh Noerono, S. Gadjah Mada University Press,
Yogyakarta.

Wang, Z. & Shmeis, R.A. 2006, Dissolution Controlled Drug Delivery System. In
Li, X. & Jasti, B.R. (ed) Design of Controlled Release Drug Delivery
System. The McGraw-Hill Companies.Inc, New York.

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