Palladium-Catalyzed Desulfitative Conjugate Addition of Aryl Sulfinic Acids and Direct ESI-MS for Mechanistic Studies

A new and efficient method for palladium­(II) catalytic desulfitative conjugate addition of arylsulfinic acids with α,β-unsaturated carbonyl compound has been developed. The key reacting intermediates including aryl Pd­(II) sulfinic intermediate, aryl Pd­(II), and COPd complexes were captured by ESI-MS/MS, which provide new experimental evidence for the understanding of addition mechanism

Table_1_Case report: Plasma cell leukemia secondary to multiple myeloma successfully treated with anti-BCMA CAR-T cell therapy.docx

Chimeric antigen receptor (CAR)-T cell therapy provides an effective salvage treatment for relapsed/refractory multiple myeloma (RRMM) patients. End-stage RRMM with plasma cell leukemia (PCL) transformation is highly aggressive and resistant to conventional therapy. There is an urgent need for new therapeutics and CAR-T therapy may play an important role. We report a case of PCL secondary to RRMM successfully treated with CAR-T cell therapy targeting B-cell maturation antigen (BCMA). A woman was diagnosed as having MM 4 years ago and progressed to secondary PCL (sPCL) of five prior lines of treatment including proteasome inhibitors, an immunomodulatory agent, cytotoxic drugs, and an anti-CD38 monoclonal antibody. After receiving a BCMA CAR-T therapy, she achieved a stringent complete response that lasted 9 months. Then, the patient irregularly took venetoclax 10 mg per day due to a slightly higher λ FLC concentration, which did not meet the criteria for progression. She maintained a complete response for the following 7 months. In conclusion, BCMA CAR-T therapy may be a promising therapeutic approach in PCL patients. More studies are needed to evaluate the benefit of anti-BCMA CAR-T therapy in PCL patients.Clinical Trial Registration:www.chictr.org.cn, ChiCTR1900024388, Registered 9 July 2019.</p

Size-Dependent Changes in Sea Spray Aerosol Composition and Properties with Different Seawater Conditions

A great deal of uncertainty exists regarding the chemical diversity of particles in sea spray aerosol (SSA), as well as the degree of mixing between inorganic and organic species in individual SSA particles. Therefore, in this study, single particle analysis was performed on SSA particles, integrating transmission electron microscopy with energy dispersive X-ray analysis and scanning transmission X-ray microscopy with near edge X-ray absorption fine structure spectroscopy, with a focus on quantifying the relative fractions of different particle types from 30 nm to 1 μm. SSA particles were produced from seawater in a unique ocean-atmosphere facility equipped with breaking waves. Changes to the SSA composition and properties after the addition of biological (bacteria and phytoplankton) and organic material (ZoBell growth media) were probed. Submicrometer SSA particles could be separated into two distinct populations: one with a characteristic sea salt core composed primarily of NaCl and an organic carbon and Mg²⁺ coating (SS-OC), and a second type consisting of organic carbon (OC) species which are more homogeneously mixed with cations and anions, but not chloride. SS-OC particles exhibit a wide range of sizes, compositions, morphologies, and distributions of elements within each particle. After addition of biological and organic material to the seawater, a change occurs in particle morphology and crystallization behavior associated with increasing organic content for SS-OC particles. The fraction of OC-type particles, which are mainly present below 180 nm, becomes dramatically enhanced with increased biological activity. These changes with size and seawater composition have important implications for atmospheric processes such as cloud droplet activation and heterogeneous reactivity

Transition Metal Associations with Primary Biological Particles in Sea Spray Aerosol Generated in a Wave Channel

In the ocean, breaking waves generate air bubbles which burst at the surface and eject sea spray aerosol (SSA), consisting of sea salt, biogenic organic species, and primary biological aerosol particles (PBAP). Our overall understanding of atmospheric biological particles of marine origin remains poor. Here, we perform a control experiment, using an aerosol time-of-flight mass spectrometer to measure the mass spectral signatures of individual particles generated by bubbling a salt solution before and after addition of heterotrophic marine bacteria. Upon addition of bacteria, an immediate increase occurs in the fraction of individual particle mass spectra containing magnesium, organic nitrogen, and phosphate marker ions. These biological signatures are consistent with 21% of the supermicrometer SSA particles generated in a previous study using breaking waves in an ocean-atmosphere wave channel. Interestingly, the wave flume mass spectral signatures also contain metal ions including silver, iron, and chromium. The nascent SSA bioparticles produced in the wave channel are hypothesized to be as follows: (1) whole or fragmented bacterial cells which bioaccumulated metals and/or (2) bacteria-derived colloids or biofilms which adhered to the metals. This study highlights the potential for transition metals, in combination with specific biomarkers, to serve as unique indicators for the presence of marine PBAP, especially in metal-impacted coastal regions

Quantification and Characterization of Fine Plastic Particles as Considerable Components in Atmospheric Fine Particles

The negative effects of air pollution, especially fine particulate matter (PM2.5, particles with an aerodynamic diameter of ≤2.5 μm), on human health, climate, and ecosystems are causing significant concern. Nevertheless, little is known about the contributions of emerging pollutants such as plastic particles to PM2.5 due to the lack of continuous measurements and characterization methods for atmospheric plastic particles. Here, we investigated the levels of fine plastic particles (FPPs) in PM2.5 collected in urban Shanghai at a 2 h resolution by using a novel versatile aerosol concentration enrichment system that concentrates ambient aerosols up to 10-fold. The FPPs were analyzed offline using the combination of spectroscopic and microscopic techniques that distinguished FPPs from other carbon-containing particles. The average FPP concentrations of 5.6 μg/m3 were observed, and the ratio of FPPs to PM2.5 was 13.2% in this study. The FPP sources were closely related to anthropogenic activities, which pose a potential threat to ecosystems and human health. Given the dramatic increase in plastic production over the past 70 years, this study calls for better quantification and control of FPP pollution in the atmosphere