Distribution and Elimination of Poly (methyl methacrylate) Nanoparticles After Subcutaneous Administration to Rats
REFERENCES (14)
- et al.
J. Pharm. Sci.
(1979) - et al.
J. Pharm. Sci.
(1981) - et al.
Infect. Immun.
(1976) - et al.
Exp. Cell Biol.
(1976) - et al.
Med. Microbiol. Immunol.
(1978) - et al.
J. Pharm. Sci.
(1981) - et al.
Infect. Immun.
(1978)
Cited by (40)
Functional PMMA nanogels by cross-linking with cyclodextrin methacrylate
2016, PolymerCitation Excerpt :The flexibility and the small size of several nanometers have raised interest [3], and have got fundamental as well as applied perspectives especially in the biomedical field [4]. In medical technologies PMMA nanoparticles are used because of the very good toxicological safety record [5], furthermore, they are slowly biodegradable [6]. PMMA nanoparticles exhibit positive adjuvant effects with some antigens [7].
Release of zirconia nanoparticles at the metal stem-bone cement interface in implant loosening of total hip replacements
2016, Acta BiomaterialiaCitation Excerpt :The abrasion-induced liberation of micron- and nanoscaled particles (PMMA and zirconia) from the bone cement mantle leads to an extreme increase in the total surface area of foreign material. Nanoscale PMMA particles have a high potential for intracellular enzymatic digestion [57–62]. The accumulation of chemically stable nanoscaled zirconia may lead to frustrated digestion, release of mediators, and apoptosis of macrophages.
Biodistribution of <sup>125</sup>I-labeled polymeric vaccine carriers after subcutaneous injection
2013, Bioorganic and Medicinal ChemistryCitation Excerpt :When Alum was injected subcutaneously into monkeys, one full year was required to clear Alum from the SOI.29 In addition, 55–77% of 14C-labeled PMMA NPs subcutaneously administered into rats still remained at the SOI even at 287 days-postinjection.39 Although γ-PGA-Phe-Tyr NPs were stable in PBS as shown in Figure 2, γ-PGA-Phe NPs, as previously reported,40 can be degraded in the presence of enzymes such as γ-glutamyl transpeptidase, lipase and some proteases, which are distributed in wide ranges of tissues.
Emerging nanomedicines for early cancer detection and improved treatment: Current perspective and future promise
2010, Pharmacology and TherapeuticsCitation Excerpt :5-FU works mainly by inhibiting thymidylate synthase, thus blocking the synthesis of thymidine, a nucleotide that is required for DNA replication. Nanoparticle-mediated delivery of 5-FU was first described by Kreuter et al. (1983) in the mid-1980s using polybutylcyanoacrylate (PBCN) nanoparticles. PBCN-bound 5-FU showed enhanced cytotoxicity against subcutaneous Crocker sarcoma S180 tumor cells in mice following intraperitoneal (i.p.) administration, and PBCN-conjugated 5-FU exhibited prolonged persistence at the tumor site as compared to pristine drug (Kreuter & Hartmann, 1983).
Enhanced circulation time and antitumor activity of doxorubicin by comblike polymer-incorporated liposomes
2007, Journal of Controlled Release