A versatile method to produce superhydrophobic fabrics by combining electrospinning and initiated chemical vapor deposition (iCVD) is reported. In this study, poly(caprolactone) (PCL) was first electrospun and then coated with a thin layer of hydrophobic polymerized perfluoroalkyl ethyl methacrylate (PPFEMA) by iCVD. The hierarchical surface roughness inherent in the PCL electrospun mats and the extremely low surface free energy of the coating layer obtained by iCVD yields stable superhydrophobicity with a contact angle of 175° and a threshold sliding angle less than 2.5° for a 20 mg droplet. This PPFEMA-coated PCL mat was also shown to exhibit at least “grade 8” oleophobicity. Hydrophobicity was demonstrated to increase monotonically with a reduction in diameter among bead-free fibers and with the introduction of a high density of relatively small diameter beads. The systematic effect of fiber morphology on superhydrophobicity was also investigated theoretically and experimentally using both beaded and bead-free fibers with diameters ranging from 600 to 2200 nm.

The overall architecture of the MC biosynthetic gene cluster in S. lavendulae has been determined. Targeted manipulation of a putative MC pathway regulator led to a substantial increase in drug production. The cloned genes should help elucidate the molecular basis for creation of the mitosane ring system, as well efforts to engineer the biosynthesis of novel natural products.

We have demonstrated the successful deposition of poly(glycidyl methacrylate) (PGMA) thin films using hot filament chemical vapor deposition (HFCVD) with tert-butyl peroxide as the initiator. The introduction of the initiator allows for film deposition at low filament temperatures (<200 degrees C) and greatly improves the film deposition rates. The retention of the pendant epoxide chemical functionality and the linear polymeric structure in the deposited films were confirmed by infrared spectroscopy and X-ray photoelectron spectroscopy. The number-average molecular weight of the PGMA films can be systematically varied from 16,000 to 33,000 by adjusting the filament temperature and flow ratio of the initiator to the precursor. The apparent activation energies observed from PGMA deposition kinetics (100.9+/-9.6 kJ/mol) and from molecular weight measurements (-54.8+/-2.0 kJ/mol) are close to the calculated overall activation energies for the polymerization rate (104.4 kJ/mol) and number-average molecular weight (-59.2 kJ/mol), which supports the hypothesis of the free radical polymerization mechanism in the HFCVD PGMA deposition.

Highlights d A living biobank of CAFs from NSCLC patients recapitulates clinical CAF heterogeneity d Therapeutic profiling of the NSCLC CAFs reveals three distinctive functional subtypes d Subtype I and II CAFs have high HGF and FGF7 expression and protect cancer cells d Subtype III CAFs associate with better clinical response and immune cell migration

Poly(N-isopropylacrylamide) was labelled using a fluorogen with an aggregation-induced emission feature by direct polymerization; the label served as a fluorogenic probe that reveals fine details in the thermal transitions in the aqueous solution of the polymer; the working mode was readily tuned between non-monotonic and monotonic by changing the labelling degree of the polymer.