16 research outputs found

    Ability of Group IVB metallocene polyethers containing dienestrol to arrest the growth of selected cancer cell lines

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Monomeric Group IVB (Ti, Zr and Hf) metallocenes represent a new class of antitumor compounds. There is literature on the general biological activities of some organotin compounds. Unfortunately, there is little information with respect to the molecular level activity of these organotin compounds. We recently started focusing on the anti-cancer activity of organotin polymers that we had made for other purposes and as part of our platinum anti-cancer effort.</p> <p>Methods</p> <p>For this study, we synthesized a new series of metallocene-containing compounds coupling the metallocene unit with dienestrol, a synthetic, nonsteroidal estrogen. This is part of our effort to couple known moieties that offer antitumor activity with biologically active units hoping to increase the biological activity of the combination. The materials were confirmed to be polymeric using light scattering photometry and the structural repeat unit was verified employing matrix assisted laser desorption ionization mass spectrometry and infrared spectroscopy results.</p> <p>Results</p> <p>The polymers demonstrated the ability to suppress the growth of a series of tumor cell lines originating from breast, colon, prostrate, and lung cancers at concentrations generally lower than those required for inhibition of cell growth by the commonly used antitumor drug cisplatin.</p> <p>Conclusion</p> <p>These drugs show great promise in vitro against a number of cancer cell lines and due to their polymeric nature will most likely be less toxic than currently used metal-containing drugs such as cisplatin. These drugs also offer several addition positive aspects. First, the reactants are commercially available so that additional synthetic steps are not needed. Second, synthesis of the polymer is rapid, occurring within about 15 seconds. Third, the interfacial synthetic system is already industrially employed in the synthesis of aromatic nylons and polycarbonates. Thus, the ability to synthesize large amounts of the drugs is straight forward.</p

    Introduction to Polymer Chemistry

    No full text
    ill.;503.;15c

    Emerging technology sustainability

    No full text

    Organometallic polymers

    No full text
    A review. A comprehensive review of organometallic polymers having various monomers, their structural characteristics and various polymn. methods is given

    Organotin Polyethers as Biomaterials

    No full text
    Organotin polyethers are easily synthesized employing interfacial polymerization systems involving the reaction of hydroxyl-containing Lewis bases and organotin halides. A wide variety of organotin-containing polymeric products have been synthesized including those derived from natural and synthetic polymers such as lignin, xylan, cellulose, dextran, and poly(vinyl alcohol). Others have been synthesized employing known drug diols such as dicumarol, DES, and dienestrol and a wide variety of synthetic diols. Included in these materials are the first water soluble organotin polymers. The organotin polyethers exhibit a wide range of biological activities. Some selectively inhibit a number of unwanted bacteria, including Staph. MRSA, and unwanted yeasts such as Candida albicans. Some also inhibit a variety of viruses including those responsible for herpes infections and smallpox. Others show good inhibition of a wide variety of cancer cell lines including cell lines associated with ovarian, colon, lung, prostrate, pancreatic and breast cancer. The synthesis, structural characterization, and biological characterization of these materials is described in this review

    Introduction to Polymer Science and Technology

    No full text

    Methods for Introducing Inorganic Polymer Concepts throughout the Undergraduate Curriculum

    No full text
    Inorganic polymers can be introduced in a variety of undergraduate courses to discuss concepts related to polymer chemistry. Inorganic polymers such as silicates and polysiloxanes are simple materials that can be incorporated into an introductory or descriptive inorganic course. Polymers based on inorganic carbon, including diamond and graphite, can likewise be used to introduce concepts related to structure–property relationships. Diamond and graphite can be discussed in more detail in an upper-division inorganic chemistry course as well as an introduction to coordination polymers and semiconducting organic polymers. Herein, these materials are briefly discussed in terms of how they can be merged into relevant coursework

    Organogermanium polymers.

    No full text
    abstract: A review. Prepn. of polygermanes (Wurtz reaction, catalytic routes, electrochem prepn.) and their chem. and phys. properties are described. Following topics are also discussed: organogermanium carbon backbone polymers, polyferrocenylgermanes, polymers contg. O, N, Si, and S in the backbone, anchored organogermanium products, stacked phthalocyanine polymers, and hyperbranched materials. [on SciFinder(R)] Cited Reference: Citations: 1) Cotton, F; Advanced Inorganic Chemistry, 5th ed 1988|2) Jurkschat, K; Organometallic Polymers of Germanium, Tin, and Lead 2002, 2|3) Lesbre, M; The Organic Compounds of Germanium 1971|4) Shibata, K; Organometallics 1998, 17, 8049|5) Mochida, K; Chem Lett 1991, 109|6) Mochida, K; Organometallics 1993, 12, 586|7) West, R; Comprehensive Organometallic Chemistry 1995, II|8) Kumada, M; Adv Organometal Chem 1968, 6, 19|9) Miller, R; Chem Rev 1989, 89, 1359|10) West, R; The Chemistry of Organo Silicon Compounds 1989|11) Bukalov, S; Macromolecules 2001, 34, 6003|12) Teramas, H; Chem Eur J 1996, 2, 529|13) Imhof, R; Chem Phys Lett 1997, 270, 500|14) Tamo, K; Angew Chem Int Ed 2000, 39, 3287|15) Tsuji, H; J Phys Chem A 2001, 105, 10246|16) Tsuji, H; J Am Chem Soc 2003, 125, 7486|17) Michl, J; Acc Chem Res 2000, 33, 821|18) Watanabe, A; Organometallics 1995, 14, 4281|19) Mochida, K; Appl Organomet Chem 1997, 11, 949|20) Mochida, K; J Organomet Chem 1997, 542, 75|21) Mochida, K; Bull Chem Soc Jpn 1997, 70, 713|22) Miller, R; ACS Symp Ser 1991, 455, 636|23) Miller, R; Polym Preprin ACS 1990, 31, 304|24) Baumert, J; Appl Phys Lett 1988, 53, 1147|25) Kodaira, T; Adv Mater 1995, 7, 917|26) Trefonas, P; J Polym Sci Polym Chem Ed 1985, 23, 2099|27) Miller, R; J Polym Sci Polym Chem Ed 1987, 25, 111|28) Mochida, K; J Organomet Chem 1994, 473, 45|29) Szymanski, W; Macromolecules 1993, 26, 869|30) Bianconi, P; Polym Preprin ACS 1990, 31, 267|31) Mochida, K; Bull Chem Soc Jpn 1996, 69, 2993|32) Yokoyama, Y; J Chem Soc Chem Commun 1995, 2275|33) Aitken, C; J Organomet Chem 1988, 349, 285|34) Reichi, J; J Am Chem Soc 1996, 118, 9430|35) Choi, N; J Organomet Chem 1998, 564, 81|36) Reichi, J; J Am Chem Soc 1996, 118, 9430|37) Kobayashi, S; Macromol Symp 1995, 98, 91|38) Kobayashi, S; Chem Lett 1993, 1385|39) Kobayashi, S; Macromolecules 1996, 29, 486|40) Neumann, W; Chem Rev 1991, 91, 311|41) Wagner, G; Organometallics 2001, 20, 418|42) Jutzi, P; Organometallics 2001, 20, 42|43) Ossig, G; Organometallics 1997, 16, 2116|44) Benet, S; Organometallics 1999, 18, 389|45) Simons, R; Organometallics 1997, 16, 1920|46) Aeiyach, S; Synth Met 1993, 58, 267|47) Martins, L; Appl Organomet Chem 1997, 11, 583|48) Hengge, E; Angew Chem Int Ed Engl 1976, 15, 370|49) Hengge, E; Monatsh Chem 1978, 109, 1217|50) Hengge, E; J Organomet Chem 1981, 212, 155|51) Shono, T; J Chem Soc Chem Commun 1990, 1160|52) Shono, T; J Chem Soc Chem Commun 1992, 896|53) Shono, T; J Org Chem 1992, 57, 1061|54) Kashimura, S; Tetrahedron Lett 1995, 36, 4805|55) Shono, T; J Org Chem 1992, 57, 5561|56) Kashimura, S; J Org Chem 1999, 64, 6615|57) Castel, A; J Organomet Chem 1983, 247, 149|58) Miller, R; Angew Chem Int Ed Engl Adv Mater 1989, 28, 1733|59) Okano, M; Electrochim Acta 1998, 44, 659|60) Kishida, H; Appl Phys Lett 1994, 65, 1358|61) Okano, M; Electrochim Acta 1999, 44, 3475|62) Ishifune, M; J Organometal Chem 2000, 611, 26|63) Hallmark, V; Macromolecules 1990, 23, 2346|64) Takeda, K; J Am Chem Soc 1990, 112, 5043|65) Takeda, K; Phys Rev B 1989, 39, 11028|66) Tada, T; J Phys Chem 1993, 97, 1019|67) Vogg, G; Adv Mat 2000, 12, 1278|68) Creemers, H; J Organometal Chem 1967, 7, 237|69) Ruidisch, I; J Organometal Chem 1963, 1, 160|70) Mercuri, F; J Mol Struct Thermochem 1999, 489, 35|71) Mochida, K; Polyhedron 1998, 17, 3963|72) Hayashi, T; Chem Lett 1992, 647|73) Hockenmeyer, J; Appl Organomet Chem 1997, 11, 513|74) Ritter, S; Chem Mater 1992, 4, 872|75) Brefort, J; J Organomet Chem 1994, 464, 133|76) Sohn, H; J Am Chem Soc 2003, 125, 3821|77) Lucht, B; Organometallics 2000, 19, 3469|78) Gomez, F; Organomet Chem 1999, 592, 271|79) Kobayashi, S; Chem Lett 1993, 25|80) Kobayashi, S; J Am Chem Soc 1990, 112, 1625|81) Kobayashi, S; J Am Chem Soc 1995, 117, 2187|82) Mazerolles, P; J Organometal Chem 1966, 5, 35|83) Zhang, X; Macromolecules 1988, 21, 1563|84) Gerasimov, G; Macromol Chem Phys 1998, 199, 2179|85) Small, J; ACS Sym Ser (Hybrid Organic-Inorganic Composites) 1995, 585|86) Schroeder, H; Inorganic Chem 1969, 8, 2444|87) Lesbre, M; Compt Rend C 1963, 257, 2302|88) Foucher, D; Organometallics 1994, 13, 4959|89) Reddy, N; J Chem Soc Chem Commun 1995, 2263|90) Peckham, T; Macromolecules 1996, 29, 2396|91) Kapoor, R; Organometallics 1995, 14, 4944|92) Espada, L; Organometallics 2002, 21, 3758|93) Carraher, C; Makromol Chem 1971, 141, 245|94) Carraher, C; J Polymer Sci A! 1972, 10, 413|95) Carraher, C; Angew Makromol Chemie 1973, 31, 115|96) Carraher, C; J Appl Polym Sci 1976, 20, 2255|97) Kobayashi, S; J Am Chem Soc 1994, 116, 6047|98) Kobayashi, S; J Am Chem Soc 1992, 114, 4929|99) Kobayashi, S; Adv Mater 1993, 5, 57|100) Riviere, R; J Organomet Chem 1975, 97, C37|101) Nishikubo, T; Macromolecules 1996, 29, 5529|102) Akira, I; JP 57145888 1982|103) Satge, J; J Organometal Chem 1969, 16, 71|104) Satge, J; Compt Rend (C) 1967, 265, 494|105) Massol, M; Compt Rend (C) 1969, 268, 1710|106) Yoder, C; J Amer Chem Soc 1966, 88, 2170|107) Yoder, C; J Amer Chem Soc 1966, 88, 4831|108) Davidson, W; J Organometal Chem 1965, 3, 285|109) Shoda, S; Macromol Chem Phys 1996, 197, 2437|110) Sanji, T; Chem Lett 1999, 547|111) Tagle, L; J Macromol Sci A Pure Appl Chem 2000, 37, 997|112) Tagle, L; J Inorg Organomet Polym 2000, 10, 73|113) Polyakova, A; Dokl Akad Nauk SSSR 1960, 130, 1037|114) Korshak, V; Dokl Akad Nauk SSSR 1959, 128, 960|115) Noltes, J; Rec Trav Chim 1961, 80, 623|116) Mochida, K; Polyhedron 1997, 16, 1767|117) Pluckett, N; J Org Chem 1997, 62, 2885|118) Spivey, A; Chem Commun 1999, 835|119) Cho, O; Macromolecules 1990, 23, 12|120) Spivey, A; J Org Chem 2000, 65, 5253|121) Marks, T; Inorganic and Metal-Containing Polymeric Materials 1990|122) Law, C; Inorg Organomet Polym. In pres
    corecore