PubMed Health⌕ Search

Biomedical subjects

H Hoeksema

Publications and source records attributed to H Hoeksema.

17 recordsLinked to original sources

A conservative approach for deep dermal burn wounds using polarised-light therapy.

This article reports a clinical study investigating the role of polarised-light therapy in the conservative treatment of deep dermal burn wounds. In 22 out of 67 patients with deep dermal burn wounds, clinical evaluation revealed only a very limited potential for spontaneous healing, and, despite the fact that the majority of the surgeons (four out of six) would have recommended surgery, these patients were treated conservatively with polarised-light therapy (400-2000 nm, 40 m W cm(-2), 2.4 J cm(-2)) until complete closure. Evaluation by a panel of four surgeons, all experts in burn surgery, revealed that conservative treatment of these deep dermal wounds with polarised-light irradiation resulted in a significantly shorter healing time, with almost no hypertrophic scarring, and optimal aesthetic and functional results at long-term follow-up. No extension of the hospital stay was required. Polarised-light therapy may be a valuable way of avoiding surgery in patients with deep dermal burns.

Adolescent↗

Isolation and characterization of a new antibiotic U-62162.

A new antibiotic U-62162 has been isolated from the fermentations of Streptomyces verdensis Dietz, sp. n. (UC-8157). The compound has been characterized and its gross structure has been elucidated. The antibiotic inhibited the growth of Gram-positive bacteria (particularly Staphylococcus aureus) but was inactive in experimentally infected animals.

Animals↗

The chemistry of the rubradirins. I. The structures of rubransarols A and B.

The antibiotic rubradirin, C48H46N4O20 was cleaved at an ester function by aqueous methylamine into rubransarol A, C23H23NO8, and a methyl amide, C26H28N4O12. Rubradirin B, C40H33N3O15, was similarly cleaved in methanolic ammonia into rubransarol B, C23H23NO8, and the primary amide, C17H13N3O7. The rubransarols are shown to be unique ansamycins which are isomeric at a double bond in the large ring.

Anti-Bacterial Agents↗

Biomodification of albocycline by Streptomyces venezuelae.

The macrolide antibiotic albocycline, when added to the fermentations of Streptomyces venezuelae UC-2560 (WC-3627) underwent a gradual loss of antimicrobial activity. The inactive product of this biotransformation was isolated from the fermentations and was shown to be 2,3-dihydroalbocycline.

Anti-Bacterial Agents↗

The isolation and characterization of rubradirin B.

Rubradirin B, C40H33N3O15, was separated from other components of the rubradirin complex by chromatographic and crystallization procedures. The spectrum of antibacterial activity is similar to that of rubradirin, but the antibiotic is less active.

Animals↗

Reduction products of spectinomycin.

The two epimers of dihydrospectinomycin have been separated and identified structurally. Four tetrahydrospectinomycins have also been prepared.

Animals↗