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A fully calibrated strategy has been investigated for the first time for the accurate determination of absolute isotopic composition and atomic weight of molybdenum using multiple-collector inductively coupled plasma mass spectrometry. The correction for instrumental mass bias was performed using synthetic isotope mixtures, which were gravimetrically prepared with all of the seven high-purity and isotopically enriched molybdenum isotope materials together. Six natural molybdenum materials, including molybdenum standard solution NIST SRM 3134, were accurately measured and yielded the absolute isotopic composition (in atom %, k = 1) of [sup 92]Mo-14.690(18), [sup 94]Mo-9.173(6), [sup 95]Mo-15.865(5), [sup 96]Mo-16.666(3), [sup 97]Mo-9.588(4), [sup 98]Mo-24.307(16), and [sup 100]Mo-9.711(13). These isotopic data enable an atomic weight A[sub r](Mo) of 95.9466(34) (k = 2) to be calculated, which is slightly lower than the current standard atomic weight 95.95(1) and with a much improved uncertainty. The associated uncertainties were evaluated according to the Guide to Expression of Uncertainty in Measurement of ISO/BIPM and Monte Carlo simulation to ensure that all sources of uncertainty were fully accounted for. A particular characteristic of the proposed new approach is that mass bias correction factor K for each isotope ratio of molybdenum can be achieved via fully experimental determination without using the traditional semiempirical correction mathematical models. In addition, the relationship between mass of isotope and bias per mass unit β was investigated based on the thorough measurement data. [ABSTRACT FROM AUTHOR]

In this work, two methods with complementary features, catalytic and molecular beacon (CAMB) and label-free fluorescent sensors using an abasic site, have been combined into new label-free CAMB sensors that possess advantages of each method. The label-free method using a dSpacer-containing molecular beacon makes CAMB more cost-effective and less interfering with the catalytic activity, while CAMB allows the label-free method to use true catalytic turnovers for signal amplifications, resulting in a new label-free CAMB sensor for Pb2+ ion, with a detection limit of 3.8 nM while maintaining the same selectivity. Furthermore, by using CAMB to overcome the label-free method's limitation of requiring excess enzyme strands, a new label-free CAMB sensor using aptazyme is also designed to detect adenosine down to 1.4 μM, with excellent selectivity over other nucleosides. [ABSTRACT FROM AUTHOR]