AIM OF THE STUDY Based on their experience using Versajet for debridement of chronic wounds, the Authors set up a study protocol to verify whether the hydro-surgical cleansing could offer the possibility of taking tissue specimens suitable for diagnostic microbiological evaluation. The aims of the study were the following: MAIN PURPOSE To evaluate the efficacy of hydro-surgery in detecting th...

Figure S1: molecules used to chemically functionalize the surfaces. To the left, 3-Aminopropyl)-triethoxysilane (APTES). To the right, poly-L-lysine hydro bromide. Figure S2: Morphological AFM images. Scale bar is 10 µm A: Si/SiO 2 coated with 3-Aminopropyl)-triethoxysilane (APTES), B: Si/SiO 2 coated with, poly-L-lysine hydro bromide and C: Bare Si/SiO 2 .

The structure of the racemic title compound, C(10)H(15)NO(4), consists of a tricyclic skeleton comprising a six-membered piperidine ring and five-membered isoxazolidine and tetra-hydro-furan rings. The piperidine ring adopts a distorted chair conformation, while the isoxazolidine and tetra-hydro-furan rings have envelope conformations.

In the title compound, C(19)H(22)N(4)O(2), the tetra-hydro-pyrimidine ring adopts an envelope conformation (with the N atom connected to the benzyl group representing the flap). This benzyl group occupies a quasi-axial position. The two benzyl groups lie over the tetra-hydro-pyridimidine ring. The amino group is a hydrogen-bond donor to the nitro group.

The innovative design and synthesis of nanofiber based hydro-philic/phobic membranes with a thin hydro-phobic nanofiber layer on the top and a thin hydrophilic nanofiber layer on the bottom of the conventional casted micro-porous layer which opens up a solution for membrane pore wetting and improves the pure water flux in membrane distillation.

The title limonoid 14-de-oxyxyloccensin K, C(27)H(34)O(7), isolated from Chisocheton ceramicus (Meliaceae), features an oxygen linkage between carbon-3 and carbon-8 along with a tetra-hydro-furyl sub-unit. The six-membered rings adopt chair configurations and the tetra-hydro-furyl sub-unit has an envelope shape.

In the title compound, C14H14O4, the dihedral angle between the hydro-furan and benzene rings is 88.41 (15)°. The hydro-pyran ring adopts an envelope conformation, with the O-bound methyl-ene C atom as the flap. In the crystal, weak aromatic π-π stacking is observed [centroid-centroid separation = 3.848 (2) Å].

In the title compound, C13H15N3S, the 4,5-di-hydro-3H-1,2,4-triazole ring is nearly planar [maximum deviation = 0.020 (1) Å], while the cyclo-hexane ring adopts a chair conformation. The dihedral angle between the 4,5-di-hydro-3H-1,2,4-triazole ring and the phenyl ring is 74.68 (7)°. No specific inter-molecular inter-actions are discerned in the crystal packing.

The title adamantane derivative, C(19)H(25)NO(2), was synthesized as part of a study into potential anti-tuberculosis agents. The adamantane skeleton displays shorter than normal C-C bond lengths ranging between 1.5230 (15) and 1.5329 (16) Å. The structure displays O-H⋯O hydrogen bonding and an inter-digitated layered packing structure with distinct hydro-philic and hydro-phobic regions.