-
2
-
-
66149152564
-
Characterization and application of new hyper-cross-linked cyclodextrins
-
Trotta F., and Cavalli R. Characterization and application of new hyper-cross-linked cyclodextrins. Compos. Interfaces 16 (2009) 39-48
-
(2009)
Compos. Interfaces
, vol.16
, pp. 39-48
-
-
Trotta, F.1
Cavalli, R.2
-
5
-
-
84870948920
-
-
Turin, May
-
P.R. Vavia, S. Swaminattan, F. Trotta, R. Cavalli, Applications of Nanosponges in Drug Delivery XIII International Cyclodextrin Symposium, Turin 14-17, May 2006.
-
(2006)
Applications of Nanosponges in Drug Delivery XIII International Cyclodextrin Symposium
, pp. 14-17
-
-
Vavia, P.R.1
Swaminattan, S.2
Trotta, F.3
Cavalli, R.4
-
6
-
-
75449092118
-
-
M Pharm. Sci. Thesis, University of Mumbai, India, July
-
S. Swaminathan, Studies on Novel Dosage Forms, M Pharm. Sci. Thesis, University of Mumbai, India, July 2006.
-
(2006)
Studies on Novel Dosage Forms
-
-
Swaminathan, S.1
-
7
-
-
0024324205
-
On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complex
-
Hertzberg R.P., Caranfa M.J., and Hecht S.M. On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complex. Biochemistry 28 (1989) 4629-4638
-
(1989)
Biochemistry
, vol.28
, pp. 4629-4638
-
-
Hertzberg, R.P.1
Caranfa, M.J.2
Hecht, S.M.3
-
8
-
-
0030055094
-
Current perspectives on camptothecin in cancer treatment
-
Dancey J., and Eisenhauer E.A. Current perspectives on camptothecin in cancer treatment. Br. J. Cancer 74 (1996) 327-338
-
(1996)
Br. J. Cancer
, vol.74
, pp. 327-338
-
-
Dancey, J.1
Eisenhauer, E.A.2
-
11
-
-
7144248725
-
Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca accuminata
-
Wall M.E., Wani M.C., Cook C.E., Palmer K.H., McPhail A.T., and Sim G.A. Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca accuminata. J. Am. Chem. Soc. 88 (1966) 3888-3890
-
(1966)
J. Am. Chem. Soc.
, vol.88
, pp. 3888-3890
-
-
Wall, M.E.1
Wani, M.C.2
Cook, C.E.3
Palmer, K.H.4
McPhail, A.T.5
Sim, G.A.6
-
12
-
-
0022340594
-
Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I
-
Hsiang Y.H., Hertzberg R., Hecht S., and Liu L.F. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I. J. Biol. Chem. 260 (1985) 14873-14878
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 14873-14878
-
-
Hsiang, Y.H.1
Hertzberg, R.2
Hecht, S.3
Liu, L.F.4
-
13
-
-
0027096415
-
A kinetic and mechanistic study of the hydrolysis of camptothecin and some analogues
-
Fassberg J., and Stella V.J. A kinetic and mechanistic study of the hydrolysis of camptothecin and some analogues. J. Pharm. 81 (1992) 676-684
-
(1992)
J. Pharm.
, vol.81
, pp. 676-684
-
-
Fassberg, J.1
Stella, V.J.2
-
14
-
-
0032473430
-
Kinetics of lactone hydrolysis in antitumor drugs of camptothecin series as studied by fluorescence spectroscopy
-
Chourpa I., Millot J.M., Sockalingum G.D., Riou J.F., and Manfait M. Kinetics of lactone hydrolysis in antitumor drugs of camptothecin series as studied by fluorescence spectroscopy. Biochim. Biophys. Acta 1379 (1998) 353-366
-
(1998)
Biochim. Biophys. Acta
, vol.1379
, pp. 353-366
-
-
Chourpa, I.1
Millot, J.M.2
Sockalingum, G.D.3
Riou, J.F.4
Manfait, M.5
-
15
-
-
0027276081
-
Lipid bilayer partitioning and stability of camptothecin drugs
-
Burke T.G., Mishra A.K., Wani M.C., and Wall M.E. Lipid bilayer partitioning and stability of camptothecin drugs. Biochemistry 32 (1993) 5352-5364
-
(1993)
Biochemistry
, vol.32
, pp. 5352-5364
-
-
Burke, T.G.1
Mishra, A.K.2
Wani, M.C.3
Wall, M.E.4
-
16
-
-
0036803284
-
Camptothecin delivery methods
-
Hatefi A., and Amsden B. Camptothecin delivery methods. Pharm. Res. 19 (2002) 1389-1399
-
(2002)
Pharm. Res.
, vol.19
, pp. 1389-1399
-
-
Hatefi, A.1
Amsden, B.2
-
17
-
-
0030772855
-
Stabilization of 10-hydroxycamptothecin in poly(lactide-co-glycolide) microsphere delivery vehicles
-
Scenderova A., Burke T., and Schwendeman S. Stabilization of 10-hydroxycamptothecin in poly(lactide-co-glycolide) microsphere delivery vehicles. Pharm. Res. 14 10 (1997) 1406
-
(1997)
Pharm. Res.
, vol.14
, Issue.10
, pp. 1406
-
-
Scenderova, A.1
Burke, T.2
Schwendeman, S.3
-
18
-
-
0031573854
-
Formulation study for the antitumor drug camptothecin: liposomes, micellar solutions and a microemulsion
-
Cortesi R., Esposito E., Maietti A., Menegatti E., and Nastruzzi C. Formulation study for the antitumor drug camptothecin: liposomes, micellar solutions and a microemulsion. Int. J. Pharm. 159 (1997) 95-103
-
(1997)
Int. J. Pharm.
, vol.159
, pp. 95-103
-
-
Cortesi, R.1
Esposito, E.2
Maietti, A.3
Menegatti, E.4
Nastruzzi, C.5
-
19
-
-
34250810241
-
Preparation and antitumor characteristics of PLA/(PEG-PPG-PEG) nanoparticles loaded with camptothecin
-
Kunii R., Onishi H., and Machida Y. Preparation and antitumor characteristics of PLA/(PEG-PPG-PEG) nanoparticles loaded with camptothecin. Eur. J. Pharm. Biopharm. 67 (2007) 9-17
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.67
, pp. 9-17
-
-
Kunii, R.1
Onishi, H.2
Machida, Y.3
-
20
-
-
70349992906
-
Design and development of IT-101, a cyclodextrin containing polymer conjugate of camptothecin
-
Davis M.E. Design and development of IT-101, a cyclodextrin containing polymer conjugate of camptothecin. Adv. Drug Deliv. Rev. 61 (2009) 1189-1192
-
(2009)
Adv. Drug Deliv. Rev.
, vol.61
, pp. 1189-1192
-
-
Davis, M.E.1
-
21
-
-
51349092516
-
Development and evaluation of lipid nanoparticles for camptothecin delivery: a comparison of solid lipid nanoparticles, nanostructured lipid carriers, and lipid emulsion
-
Huang Z., Hua S., Yang Y., and Fang J. Development and evaluation of lipid nanoparticles for camptothecin delivery: a comparison of solid lipid nanoparticles, nanostructured lipid carriers, and lipid emulsion. Acta Pharmacol. Sinica 9 (2008) 1094-1102
-
(2008)
Acta Pharmacol. Sinica
, vol.9
, pp. 1094-1102
-
-
Huang, Z.1
Hua, S.2
Yang, Y.3
Fang, J.4
-
22
-
-
9644301058
-
A novel non-toxic camtothecin formulation for cancer chemotherapy
-
Barrada M., Serreqi A., Dabbarh F., Owusu A., Gupta A., and Lehnert S. A novel non-toxic camtothecin formulation for cancer chemotherapy. Biomaterials 26 (2005) 2115-2120
-
(2005)
Biomaterials
, vol.26
, pp. 2115-2120
-
-
Barrada, M.1
Serreqi, A.2
Dabbarh, F.3
Owusu, A.4
Gupta, A.5
Lehnert, S.6
-
23
-
-
57049152398
-
Acoustically active perfluorocarbon nanoemulsions as drug delivery carriers for camptothecin: drug release and cytotoxicity against cancer cells
-
Fang J., Hung C., Hua S., and Hwang T. Acoustically active perfluorocarbon nanoemulsions as drug delivery carriers for camptothecin: drug release and cytotoxicity against cancer cells. Ultrasonics 49 (2009) 39-46
-
(2009)
Ultrasonics
, vol.49
, pp. 39-46
-
-
Fang, J.1
Hung, C.2
Hua, S.3
Hwang, T.4
-
24
-
-
0036181890
-
Cyclodextrin complexation: influence on solubility, stability and cytotoxicity of camptothecin
-
Kang J., Kumar V., Yang D., Chowdhury P.R., and Hohl R.J. Cyclodextrin complexation: influence on solubility, stability and cytotoxicity of camptothecin. Eur. J. Pharm. Sci. 15 (2002) 163-170
-
(2002)
Eur. J. Pharm. Sci.
, vol.15
, pp. 163-170
-
-
Kang, J.1
Kumar, V.2
Yang, D.3
Chowdhury, P.R.4
Hohl, R.J.5
-
25
-
-
5344230687
-
Effect of hydroxypropyl-β-cyclodextrin-complexation and pH on solubility of camptothecin
-
Saetern A., Nguyen N., Bauer-Brandl A., and Brandl M. Effect of hydroxypropyl-β-cyclodextrin-complexation and pH on solubility of camptothecin. Int. J. Pharm. 284 (2004) 61-68
-
(2004)
Int. J. Pharm.
, vol.284
, pp. 61-68
-
-
Saetern, A.1
Nguyen, N.2
Bauer-Brandl, A.3
Brandl, M.4
-
26
-
-
36949025736
-
A novel polyrotaxane-based intracellular deliery system for camptothecin: in vitro feasibility
-
Moon C., Kwon Y., Lee W., Park Y., Chang L., and Yang V. A novel polyrotaxane-based intracellular deliery system for camptothecin: in vitro feasibility. J. Biomedical Mat. Res. Part A 84 (2008) 238-246
-
(2008)
J. Biomedical Mat. Res. Part A
, vol.84
, pp. 238-246
-
-
Moon, C.1
Kwon, Y.2
Lee, W.3
Park, Y.4
Chang, L.5
Yang, V.6
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