• Title/Summary/Keyword: H.283

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An Implementation of H.283 Remote Device Control in H.323 (H.323에서 운용되는 H.283 원격기기제어의 구현)

  • 성동수;이건배
    • Journal of Korea Multimedia Society
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    • v.5 no.3
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    • pp.239-248
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    • 2002

  • International Standard Organizations such as ITU(International Telecommunication Union) and IETF (Internet Engineering Task Force) are proceeding standardization for various applications and protocols to provide video-conference and multimedia conference services on a variety of networks. Remote device control among these protocols is provided with various capabilities as well as device control to multimedia conference. This protocol for remote device control is standardizing as H.282 recommendation which is specified as core service for the configuration and control of remote device to multimedia conference. The H.282 recommendation does not specify the use of a particular transport protocol. That is, T.120 multimedia conference uses T.136 and H.323 video conference uses H.283 for the transport of H.282 protocol. The introduced system in this paper is based on H.282 and is implemented to be capable of remote device control within the framework of H.323 using H.283. Also, it is shown that a variety of services in the specification of the standard are satisfied through experiments.

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Interaction Characteristics of Nucleoside Analogues with Human Organic Anion Transporter 1 and 3

  • Choi, Jun-Shik;Cheon, Eun-Pa;Han, Hyo-Kyung
    • Journal of Pharmaceutical Investigation
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    • v.36 no.4
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    • pp.283-286
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    • 2006

  • The present study aimed to investigate the interaction of nucleoside analogs with human organic anion transporter 1 and 3(hOAT1 and hOAT3) that play a primary role in the tubular uptake of endogenous and exogenous organic anions in the kidney. The interactions of ddC, ara-C, ara-A and ara-U with hOAT1 and hOAT3 were examined using MDCK cells stably overexpressing hOAT1 or hOAT3. Among the tested drugs, ddC showed the highest affinity to hOAT1 with $IC_{50}$ values of 5.2 mM, while ara-A, ara-C and ara-U weakly inhibited the cellular uptake of $[^3H]-PAH$ in MDCK-hOAT1 cells at 1 mM. In contrast, all the tested drugs did not have any inhibition effect on the cellular uptake of $[^3H]-estrone$ sulfate in MDCK-hOAT3 cells over the drug concentration of 0.01-2 mM, implying that they might not interact with hOAT3. Taken all together, the present study suggests that hOAT1 could weakly interact with nucleoside analogues such as ddC, ara-C, ara-A and ara-U but the interaction with hOAT3 during the urinary excretion of these nucleoside analogues may be negligible in the kidney.

  • https://doi.org/10.4333/KPS.2006.36.4.283 인용 PDF KSCI