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Mahsa Shirzadian Gilan Behrouz Maham 《International Journal of Communication Systems》2023,36(5):e5427
One of the main imperfections degrading the performance of full-duplex (FD) relaying systems is the outage floor. In this work, a power scaling method is proposed, which overcomes this effect even when there does not exist a direct channel between source and destination nodes. The system is composed of decode-and-forward (DF) FD relays over the Nakagami-m fading environment. To promote system performance, joint antenna and relay selection methods are employed in the FD relaying systems. Each FD relay is equipped with multiple antennas for receiving and the other for transmitting the information. The transmitting and receiving antennas are chosen based on the instantaneous channel variations, and one relay is selected to improve the signal-to-interference and noise ratio (SINR) of the FD relaying system. The performance of the proposed design is investigated. Moreover, the closed-form equations of the ergodic capacity and outage probability are attained. The analytical results are confirmed by different simulations. Results indicate that the proposed design achieves an additional spatial diversity gain because of using the antenna selection at the relay nodes. Moreover, by power scaling (PS) method, the system performance is effectively improved compared to the conventional FD relaying structures. 相似文献
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Xi Chen Shima Gholizadeh Mahsa Ghovvati Ziqing Wang Marcus J. Jellen Azadeh Mostafavi Reza Dana Nasim Annabi 《American Institute of Chemical Engineers》2023,69(6):e18067
Ocular inflammation is commonly associated with eye disease or injury. Effective and sustained ocular delivery of therapeutics remains a challenge due to the eye physiology and structural barriers. Herein, we engineered a photocrosslinkable adhesive patch (GelPatch) incorporated with micelles (MCs) loaded with loteprednol etabonate (LE) for delivery and sustained release of drug. The engineered drug loaded adhesive hydrogel, with controlled physical properties, provided a matrix with high adhesion to the ocular surfaces. The incorporation of MCs within the GelPatch enabled solubilization of LE and its sustained release within 15 days. In vitro studies showed that MC loaded GelPatch supported cell viability and growth. In addition, subcutaneous implantation of the MC loaded GelPatch in rats confirmed its in vivo biocompatibility and stability within 28 days. This non-invasive, adhesive, and biocompatible drug eluting patch can be used as a matrix for the delivery and sustained release of hydrophobic drugs. 相似文献