284x Filetype PDF File size 0.02 MB Source: eprints.ums.ac.id
50
DAFTARPUSTAKA
Anonim, 1979, Farmakope Indonesia, Edisi III, 7, Departemen Kesehatan Republik
Indonesia, Jakarta.
Anonim, 1995, Farmakope Indonesia, Edisi IV, 175, 783-784, Departemen
Kesehatan Republik Indonesia, Jakarta.
Ansel, H.C., Allen, L.V., and Popovich, N.G., 1999, Pharmaceutical Dosage Forms
and Drug Delivery System, Edisi VII, 229-243, Lippincott Williams &
Wilkins a Wotters Kluver Company, Philadelphia-Baltimare-New York-
London-Buenos Aires-Hongkong-Sydney-Tokyo.
Armstrong, N.A, and James, K.C., 1996, Pharmaceutical Experimental Design and
Interpretation, 205-222, Taylor and Francis Publisher, London.
Banker, G.S. and Rhodes, C.T., 1995, Modern Pharmaceutics, Third Edition, 576,
Marcel Dekker Inc, New York-Basel.
Bodmeier, R., dan Siepmann, J., 1999, Nondegradable Polymer For Drug Delivery,
dalam Mathiowitz, Encylopedia of Controlled Drug Delivery,VolI,
AWiley-Interscience Publication, Canada.
Bolton, S., 1997, Pharmaceutical Statistics: Practical and Clinical Applications,
Third Edition, 592-595, Marcel Dekker Inc, New York-Basel.
Conrad, J.M., and Robinson, J.R., 1987, Sustained Release Through Coating,
in Lachman, L., Lieberman, H. A., Pharmaceuticals Dosage Forms Tablets,
Vol III, 156-157, Marcel Dekker Inc, New York.
Jantzen,G.M., and Robinson, J.R., 1996, Sustained and Controlled-Release Drug
Delivery Systems, in Banker, G.S., Rhodes, C.T., (Eds), Modern
Pharmaceutics, Edisi III, 575-609, Marcel Dekker Inc., New York-Basel-
Hongkong.
Khan, G., and Hayer, B.A., 1973, Physic Chemical Basis of the Buffered
Acetylsalicylic Acid Controversy, 262, 1053-1058, New England. J. Med.
Lachman, L., Lieberman, H.A., dan Kanig, J.L., 1994, Teori dan Praktek Industri
Farmasi II, diterjemahkan oleh Siti Suyatmi dan Iis Aisyah, Edisi III,
934-935, UI Press, Jakarta.
Lordi, N.G., 1976, Sustained Release Dosage Forms, in Lachman, L., Lieberman,
H.A., Kanig, J.L., The Theory and Practice of Industrial Pharmacy,
2nd Edition, 430-456, Lea and Febriger, Philadelphia.
50
51
Martin, A., Swarbrick, J., dan Cammarata, A., 1983, Farmasi Fisik, diterjemahkan
oleh Yoshita dan Iis Aisyah, Edisi III, 845-858, UI Press, Jakarta.
Martin, A., Bustamante, P. and Chun, A.H.C., 1993, Physical Pharmacy,
Fourth Edition, 331-336, Lea & Febiger, Philadelphia, London.
Martodiharjo, S., 1996, Pelepasan Teofilin Secara Terkontrol dari Matriks
Hidroksipropil Metilselulosa Viskositas Tinggi, Vol 7, No. 3, 153-159
Majalah Farmasi Indonesia.
th
Parfitt, K., 1999, Martindale the Complete Drug Reference, 13 Edition, 765-773,
1471-1475, Pharmaceutical Press.
Parrott, E.L., 1971, Pharmaceutical Technology Fundamental Pharmaceutics,
Edisi III, 92-108, 158, Burgess Publishing Company, Minneapolis.
Rowe, R.C., Sheskey, P.J., and Owen, S.C., 2006, Handbook of Pharmaceutical
th
Excipients, 5 Edition, 278-282, 346-349, Pharmaceutical Press, London.
Rustamaji dan Suryawati, S., 2000, Kepentingan Penelitian dan Ketersediaan Hayati
Terhadap Sediaan Lepas Lambat Teofilin, Pertemuan Ilmiah Khusus
Perhimpunan Dokter Paru Indonesia, Semarang, 7-8 Juli 2000.
Shargel, L., Wu-Pong, S., and Yu, A.B.C., 2005, Applied Biopharmaceutics and
th
Pharmacokinetics, 5 Edition, 528-530, 548, Mc-Graw-Hill.
Simon, B.H., 1999, Teknologi Sediaan Farmasi Sustained Release Oral,
Vol. 12, No. 4, 20, Dexa Media.
Simon, B.H., 2001, Tablet dan Kapsul Lepas Lambat (Sustained Release), Vol. 141,
No. 3, 118-120, Dexa Media.
Voigt, R., 1984, Buku Pelajaran Teknologi Farmasi, Diterjemahkan oleh Suwandi,
S.N., 341-361, UI Press, Jakarta,
Wagner, J. G., 1971, Biopharmaceutics and Relevant Pharmacokinetics,EdisiI,
98-157, Drug Intellegen Publication, Hamilton.
no reviews yet
Please Login to review.