Literature DB >> 7790047

The effect of molecular weight and gel preparation on humoral adjuvancy of silicone oils and silicone gels.

J O Naim1, K M Ippolito, R J Lanzafame.   

Abstract

Silicone gels from commercial breast implants have been shown previously by our laboratory to be potent humoral adjuvants, while the low molecular size 20 centistoke (cs) silicone oil (M.W. 1900) possesses no measurable adjuvant properties. It became necessary to shear the silicone gel during our previous experiments in order to facilitate injection through a syringe and needle, it is conceivable that shearing may reduce the molecular weight of the silicone gel used. This investigation was undertaken to determine whether humoral adjuvancy of silicone oils is dependent on molecular weight and whether the method of shearing the silicone gel affects its adjuvancy. Four Dow Corning 360 Medical silicone oils (100 cs, M.W. approximately 5,000; 350 cs, M.W. approximately 10,000; 1000 cs, M.W. approximately 16,500 and 12,500 cs, M.W. approximately 60,000) and Dow Corning octamethylcyclotetrasiloxane (D4, M.W. 296) were tested for their humoral adjuvancy by immunizing 64 Sprague Dawley rats with 50 micrograms of bovine serum albumin (BSA) mixed with each oil. The rats were periodically bled and the sera were analyzed for anti-BSA antibodies by ELISA. In a separate experiment, three silicone gel preparations with reproducible characteristics were prepared by using a tissue homogenizer and varying the applied shear force. Each of these preparations was tested for its humoral adjuvancy as previously described for silicone oils. Rats immunized with BSA mixed with the highest molecular size silicone oil tested (M.W. approximately 60,000) showed a significant increase in anti-BSA antibodies as compared to the lower molecular size oils. The three silicone gel preparations showed no difference in their adjuvancy effect. Thus, the humoral adjuvancy of silicone oil appears to be dependent on molecular weight. Differential shearing of the silicone gel does not alter its humoral adjuvancy.

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Year:  1995        PMID: 7790047     DOI: 10.3109/08820139509066849

Source DB:  PubMed          Journal:  Immunol Invest        ISSN: 0882-0139            Impact factor:   3.657


  4 in total

1.  Pneumonitis caused by silicone gel following breast implant rupture.

Authors:  S Paredes Vila; F J Gonzalez Barcala; J Suarez Antelo; M Moldes Rodriguez; I Abdulkader Nallib; L Valdes Cuadrado
Journal:  Ir J Med Sci       Date:  2009-06-30       Impact factor: 1.568

2.  Induction of hypergammaglobulinemia and macrophage activation by silicone gels and oils in female A.SW mice.

Authors:  J O Naim; M Satoh; N A Buehner; K M Ippolito; H Yoshida; D Nusz; L Kurtelawicz; S F Cramer; W H Reeves
Journal:  Clin Diagn Lab Immunol       Date:  2000-05

3.  Tungsten-induced denaturation and aggregation of epoetin alfa during primary packaging as a cause of immunogenicity.

Authors:  Andreas Seidl; Otmar Hainzl; Marleen Richter; Robert Fischer; Stephan Böhm; Britta Deutel; Martin Hartinger; Jörg Windisch; Nicole Casadevall; Gerard Michel London; Iain Macdougall
Journal:  Pharm Res       Date:  2011-11-18       Impact factor: 4.200

4.  Intravascular large B-cell lymphoma associated with silicone breast implant, HLA-DRB1*11:01, and HLA-DQB1*03:01 manifesting as macrophage activation syndrome and with severe neurological symptoms: a case report.

Authors:  Oswald Moling; Andrea Piccin; Martina Tauber; Peter Marinello; Mariagrazia Canova; Marco Casini; Giovanni Negri; Bernd Raffeiner; Raffaella Binazzi; Latha Gandini; Cinzia Vecchiato; Giovanni Rimenti; Atto Billio
Journal:  J Med Case Rep       Date:  2016-09-15
  4 in total

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