Rancang Bangun Sistem Simulasi Denyut Nadi Pergelangan Tangan pada Vital Sign Simulator sebagai Media Pembelajaran Keterampilan Medik Mahasiswa Kedokteran

Salah satu kompetensi yang harus dikuasai oleh mahasiswa kedokteran/calon dokter adalah keterampilan klinik. Komponen keterampilan klinik ini meliputi pemeriksaan fisik berupa tanda vital (vital sign) dari seorang pasien. Diperlukan pelatihan keterampilan pemeriksaan tanda vital khususnya denyut nadi untuk meningkatkan kompetensi calon dokter tersebut. Oleh karena itu perlu dikembangkan simulator denyut nadi pada pergelangan tangan/artery radialis berbasis simulasi pasien berupa jaket/kaos menset yang dilengkapi “sistem pintar”. Dengan demikian mahasiswa kedokteran dapat berlatih pengukuran tanda vital dengan tetap memperhatikan etika komunikasi dan profesionalisme. Pada penelitian ini rancang bangun sistem simulasi denyut nadi dengan menggunakan mikrokontroller ATMega16 dan aktuator berupa katup solenoid serta pompa udara. Data yang ditampilkan di LCD berupa pencacah denyut nadi, set point jumlah denyut nadi, dan timer.Dari penelitian ini dihasilkan rancang bangun alat simulasi denyut nadi pada pergelangan tangan/artery radialis dengan rentang 0-180 denyut/menit dan memiliki tingkat akurasi sebesar 99,98% dari metode Palpasi dan 99,95% dari metode penggunaan sensor piezoelectric

Two new 4-methylidene containing steroids, craterol A and B, from the New Zealand two sponge association between Stelletta crater and Desmacella dendyi

NMR-directed investigation of the two sponge association between Stelletta crater and Desmacella dendyi has resulted in the isolation of two new members of the rare 4-methylidene class of sterols. Craterol A (1) and B (2) represent the first examples of natural products reported from the species S. crater. The isolation of these compounds challenges the role of 4-methylidene sterols as chemotaxonomic markers for the sponge genus Theonella

Pyrroloquinoline derivatives from a Tongan specimen of the marine sponge Strongylodesma tongaensis

Pyrroloquinoline alkaloids are well known bioactive metabolites commonly found from latrunculiid sponges. Two new pyrroloquinoline alkaloids, 6-bromodamirone B (1) and makaluvamine W (2), were isolated from the Tongan sponge Strongylodesma tongaensis. Makaluvamine W (2) contains an oxazole moiety, which is rare in this large group of natural products, and is the first example of a pyrroloquinoline with nitrogen substitution at C-8. Both 1 and 2 lacked activity against a human promyelocytic leukaemia cell line (HL-60), supporting the premise that an intact iminoquinone moiety plays a key role in the cytotoxicity of this compound class. The chemotaxonomic impact of these makaluvamine-type compounds is also discussed

Zampanolides B−E from the Marine Sponge Cacospongia mycofijiensis: Potent Cytotoxic Macrolides with Microtubule- Stabilizing Activity

Four new compounds (2−5) structurally related to the microtubule-stabilizing agent (−)-zampanolide (1) have been isolated from the Tongan marine sponge Cacospongia mycofijiensis. Three of these new structures, zampanolides B−D (2−4), exhibit nanomolar cytotoxicity toward the HL-60 cell line, are antimitotic, and induce in vitro tubulin polymerization at levels comparable to 1. Zampanolide E (5), saturated at C-8/C-9, was significantly less potent and does not stabilize purified tubulin, even at 10-fold higher concentrations. The structural differences across these compounds reveal a plasticity of the zampanolide pharmacophore. While unsaturation is required at Δ8, the configuration of this alkene and those of Δ4 and Δ4′ have little effect on tubulin polymerization. The first natural co-occurrence of 1 and (−)-dactylolide (6) from the same sponge extract is also note

Pyrroloquinoline derivatives from a Tongan specimen of the marine sponge Strongylodesma tongaensis

Pyrroloquinoline alkaloids are well known bioactive metabolites commonly found from latrunculiid sponges. Two new pyrroloquinoline alkaloids, 6-bromodamirone B (1) and makaluvamine W (2), were isolated from the Tongan sponge Strongylodesma tongaensis. Makaluvamine W (2) contains an oxazole moiety, which is rare in this large group of natural products, and is the first example of a pyrroloquinoline with nitrogen substitution at C-8. Both 1 and 2 lacked activity against a human promyelocytic leukemia cell line (HL-60), supporting the premise that an intact iminoquinone moiety plays a key role in the cytotoxicity of this compound class. The chemotaxonomic impact of these makaluvamine-type compounds is also discussed

Haemolytic fungi isolated from sago starch in Papua New Guinea

Sago haemolytic disease (SHD) is a rare but often fatal illness linked to consumption of stale sago starch in Papua New Guinea. Although the aetiology of SHD remains unknown, mycotoxins are suspected. This study investigated whether fungi isolated from Papua New Guinean sago starch were haemolytic. Filamentous fungi and yeasts from sago starch were grown on sheep blood agar and some on human blood agar. Clear haemolytic activity was demonstrated by 55% of filamentous fungal isolates, but not by yeasts. A semi-quantitative bioassay was developed involving incubation of human erythrocytes with fungal extracts. Extracts of cultures of Penicillium, Aspergillus and Fusarium all caused rapid haemolysis in the bioassay. Partial fractionation of extracts suggested that both polar and non-polar haemolytic components had haemolytic activity in vitro. Further work is warranted to identify these metabolites and determine if they play a role in SHD