Recent developments in nanofabrication using ion projection lithography

Ion projection lithography (IPL) is an emerging technology and a major candidate for the next-generation lithography (NGL) designed to complement and supplement current optical lithographic techniques for future chip manufacturing. In this Review, the recent developments of IPL technology are examined with an emphasis on its ability to fabricate a wide variety of nanostructures for the semiconductor industry. Following an introduction of the uniqueness and strength of the technology, the basics of ion-source development and ion-target interactions with and without chemical enhancement are presented. The developments in equipment systems, masks, and resists are subsequently studied. The resolution of printed nanostructures and the corresponding throughput of the current system are assessed for NGL. Finally, concluding remarks are presented to summarize the strengths and weaknesses of the current technology and to suggest the scope for future improvement.     

A memristive circuit model for p-n junction diodes

A new simple lumped circuit model for junction diodes is presented. The model contains only 4 elements; namely, 2 controlled current sources, a nonlinear capacitor, and a memristor. Each component bears a simple relationship with the physical operating mechanisms inside the diode. The model is shown capable of simulating realistically the diode's dynamic behaviours under reverse, forward, and sinusoidal operating modes. Both the storage time and the fall time of the diode can be accurately predicted. The model is also shown capable of mimicking various second order effects due to conductivity modulation. In particular, the model is shown to exhibit a predominantly capacitive incremental impedance under small forward bias and a predominantly inductive impedance under large forward bias. Moreover, it includes the standard two-capacitor model as a special case.     

Activity of 2-fluoro-5-methylarabinofuranosyluracil against mouse leukemias sensitive to and resistant to 1-beta-D-arabinofuranosylcytosine

A new pyrimidine nucleoside, 2'-fluoro-5-methyl-1-beta-D-arabinofuranosyluracil, previously has been shown to be active against the herpes group of viruses in vitro and in vivo. It is also active against mouse and human leukemic cells in culture and against mouse leukemias L1210, P388, and P815 in vivo. In contrast to other 1-beta-D-arabinofuranosylcytosine (ara-C) derivatives, 2'-fluoro-5-methyl-1-beta-D-arabinofuranosyluracil, when given either i.p. or p.o., is highly active against lines of leukemias P815 and L1210 made resistant to ara-C. Against P815/ara-C and L1210/araC, it is more effective than is 5-azacytidine, a drug which has shown definite effectiveness in patients with acute leukemia whose disease has become resistant to ara-C. For these reasons, 2'-fluoro-5-methyl-1-beta-D-arabinofuranosyluracil would seem to merit clinical trial in patients with acute nonlymphocytic leukemia whose disease has become resistant to ara-C.     

Isolation and preparation of colonies grown on soft agar for ultrastructural investigation

Preparation of cell colonies grown on soft agar for electron microscopic examination is tedious. Mechanical damage to cells can occur during the process of colony removal. A procedure which permits rapid colony removal and preserves the integrity of the individual colony for ultrastructural examinations is described in this paper.     

Preparation and antimicrobial assessment of 2-thioether-linked quinolonyl-carbapenems

This reports the synthesis and in vitro antimicrobial properties of a series of 2-thioether-linked quinolonyl-carbapenems. Although the title compounds exhibited broad spectrum activity, the MICs were generally higher than those observed for selected benchmark carbapenems, quinolonyl-penems, and quinolones. Enzyme assays suggested that the title compounds are potent inhibitors of penicillin binding proteins and inefficient inhibitors of bacterial DNA-gyrase. Uptake studies indicated that the new compounds are not substrates for the norA encoded quinolone efflux pump.     

Impact of quality control on accuracy in enzyme immunoassay testing for human immunodeficiency virus type 1 antibodies

OBJECTIVE: To assess use of quality control (QC) material, supplemental to internal kit controls (calibrators), as protection against errors in enzyme immunoassay testing for human immunodeficiency virus type 1 antibodies. DESIGN: From August 1994 to January 1996, enzyme immunoassay testing accuracy was assessed for laboratories participating in the Centers for Disease Control and Prevention Model Performance Evaluation Program that provided information regarding their use of QC material. Error rates were examined for human immunodeficiency virus type 1 antibody-negative, strongly positive, and weakly positive samples. RESULTS: The overall error rate with QC (2.20%) was significantly (P = .0023) lower than the error rate without QC (2.90%). With QC use there was a significant reduction in the relative risk of error for negative (P = .014) and weakly positive (P = .0067) samples. After multivariate analysis, use of QC lowered overall error rate by 29% (P = .0009). Laboratories not using QC were at increased risk of systematic error. Following the Clinical Laboratory Improvement Amendments of 1988 guidelines for QC material was relatively more protective against error than lower frequencies/number of levels. CONCLUSIONS: Using QC protected against errors in enzyme immunoassay testing for human immunodeficiency virus type 1 antibodies. Two levels of QC should be used with each run as mandated by the Clinical Laboratory Improvement Amendments of 1988.     

Pattern synthesis of circular arrays in a moving medium

Based on a modified expression for the radiation field of a circular array in a moving medium, pattern synthesis is performed for medium motion both in the direction of and parallel to the main beam. It is shown that medium motion, even considering only first-order effects, changes the synthesized patterns significantly. The required excitation amplitudes and phases for the proper synthesis of a 21-element circular array to yield a cosine-square pattern in a moving medium are given.