VARIATIONS IN RATE OF HUMAN OSTEON FORMATION

1963 ◽  
Vol 41 (1) ◽  
pp. 19-22
Author(s):  
Elias D. Sedlin ◽  
Harold M. Frost

The authors' method depends on labelling in vivo the zone of demarcation of actively forming osteons by tetracycline antibiotics. The drugs, thus deposited in bone, are visualized by fluorescence microscopy. The label is a circular or elliptical ring whose diameter indicates the degree of completeness of the osteon at the time of drug administration. A histogram of the ring diameters therefore classifies labelled osteons as regards stage of completion at the time of drug administration. If an average formation time is assigned to osteons measured, conclusions relative to the rate of formation of the average osteon can be derived.In a histogram plotted from more than 900 labelled osteons in bones of three patients, most of the labels were concentrated in the inner half of the osteon. The authors conclude that osteon formation is initially rapid both in terms of cubic microns of bone formed in a unit time and in terms of decrease in diameter of the Haversian canal; it decreases with passage of time, and it ends with a critical minimum diameter of the Haversian canal. A 2-week cyclic variation in rate may be superimposed on the overall plot.

1963 ◽  
Vol 41 (1) ◽  
pp. 19-22 ◽  
Author(s):  
Elias D. Sedlin ◽  
Harold M. Frost

The authors' method depends on labelling in vivo the zone of demarcation of actively forming osteons by tetracycline antibiotics. The drugs, thus deposited in bone, are visualized by fluorescence microscopy. The label is a circular or elliptical ring whose diameter indicates the degree of completeness of the osteon at the time of drug administration. A histogram of the ring diameters therefore classifies labelled osteons as regards stage of completion at the time of drug administration. If an average formation time is assigned to osteons measured, conclusions relative to the rate of formation of the average osteon can be derived.In a histogram plotted from more than 900 labelled osteons in bones of three patients, most of the labels were concentrated in the inner half of the osteon. The authors conclude that osteon formation is initially rapid both in terms of cubic microns of bone formed in a unit time and in terms of decrease in diameter of the Haversian canal; it decreases with passage of time, and it ends with a critical minimum diameter of the Haversian canal. A 2-week cyclic variation in rate may be superimposed on the overall plot.


1982 ◽  
Vol 48 (01) ◽  
pp. 087-090 ◽  
Author(s):  
Carlos O Esquivel ◽  
David Bergqvist ◽  
Claes-Göran Björck ◽  
Stan N Carson ◽  
Bodil Nilsson

SummaryThe effect of sodium ibuprofen on platelet activity in vivo and the lysability of ex vivo thrombi was investigated. The formation of a hemostatic platelet plug in the rabbit mesentery and platelet embolism as a response to a laser-induced injury in the ear chamber of rabbits were used as models for determining platelet activity. Ibuprofen at a dose of 25 mg/kg i.v. was found to increase the primary (PHT) and the total hemostatic plug formation time (THT). The same dose decreased the number of cumulative emboli over a 10 min period after a laser injury to arterioles. A dose of 10 mg/kg i.v. did not affect the formation of the hemostatic platelet plug. In dogs, doses of 10, 25 und 50 mg/kg did not enhance the release of 125I-FDP from the thrombi after incubation in plasmin, but the largest dose which is approximately five times the recommended dose in humans, did significantly decrease the thrombus weight 90 and 180 min after the drug administration. In conclusion, sodium ibuprofen was shown to have an inhibitory effect on platelet function in vivo and in large doses was also found to diminish the thrombus weight.


2011 ◽  
Vol 200 (1) ◽  
pp. 47-53 ◽  
Author(s):  
Sabine Scheibe ◽  
Mario M. Dorostkar ◽  
Christian Seebacher ◽  
Rainer Uhl ◽  
Frank Lison ◽  
...  

2014 ◽  
Vol 5 (6) ◽  
pp. 1965 ◽  
Author(s):  
Jennifer A. Lee ◽  
Nikolett M. Biel ◽  
Raymond T. Kozikowski ◽  
Dietmar W. Siemann ◽  
Brian S. Sorg

2010 ◽  
Vol 1257 ◽  
Author(s):  
Andrea Fornara ◽  
Alberto Recalenda ◽  
Jian Qin ◽  
Abhilash Sugunan ◽  
Fei Ye ◽  
...  

AbstractNanoparticles consisting of different biocompatible materials are attracting a lot of interest in the biomedical area as useful tools for drug delivery, photo-therapy and contrast enhancement agents in MRI, fluorescence and confocal microscopy. This work mainly focuses on the synthesis of polymeric/inorganic multifunctional nanoparticles (PIMN) based on biocompatible di-block copolymer poly(L,L-lactide-co-ethylene glycol) (PLLA-PEG) via an emulsion-evaporation method. Besides containing a hydrophobic drug (Indomethacin), these polymeric nanoparticles incorporate different visualization agents such as superparamagnetic iron oxide nanoparticles (SPION) and fluorescent Quantum Dots (QDs) that are used as contrast agents for Magnetic Resonance Imaging (MRI) and fluorescence microscopy together. Gold Nanorods are also incorporated in such nanostructures to allow simultaneous visualization and photodynamic therapy. MRI studies are performed with different loading of SPION into PIMN, showing an enhancement in T2 contrast superior to commercial contrast agents. Core-shell QDs absorption and emission spectra are recorded before and after their loading into PIMN. With these polymeric/inorganic multifunctional nanoparticles, both MRI visualization and confocal fluorescence microscopy studies can be performed. Gold nanorods are also synthesized and incorporated into PIMN without changing their longitudinal absorption peak usable for lased excitation and phototherapy. In-vitro cytotoxicity studies have also been performed to confirm the low cytotoxicity of PIMN for further in-vivo studies.


Author(s):  
Ruiqing Ni ◽  
Zhenyue Chen ◽  
Gloria Shi ◽  
Alessia Villois ◽  
Quanyu Zhou ◽  
...  

AbstractThe abnormal deposition of beta-amyloid proteins in the brain is one of the major histopathological hallmarks of Alzheimer’s disease. Currently available intravital microscopy techniques for high-resolution plaque visualization commonly involve highly invasive procedures and are limited to a small field-of-view within the rodent brain. Here, we report the transcranial detection of amyloid-beta deposits at the whole brain scale with 20 μm resolution in APP/PS1 and arcAβ mouse models of Alzheimer’s disease amyloidosis using a large-field multifocal (LMI) fluorescence microscopy technique. Highly sensitive and specific detection of amyloid-beta deposits at a single plaque level in APP/PS1 and arcAβ mice was facilitated using luminescent conjugated oligothiophene HS-169. Immunohistochemical staining with HS-169, anti-Aβ antibody 6E10, and conformation antibodies OC (fibrillar) of brain tissue sections further showed that HS-169 resolved compact parenchymal and vessel-associated amyloid deposits. The novel imaging platform offers new prospects for in vivo studies into Alzheimer’s disease mechanisms in animal models as well as longitudinal monitoring of therapeutic responses at a single plaque level.


2021 ◽  
Author(s):  
Vanisri Raviraj ◽  
Binh T.T. Pham ◽  
Byung J. Kim ◽  
Nguyen T.H. Pham ◽  
Lai F. Kok ◽  
...  

Abstract Background: The skin is both a target and a potential conduit for the delivery of drugs, but its cornified cell layer resists penetration by most molecules. This study investigated the potential of superparamagnetic iron oxide nanoparticles to facilitate the transdermal delivery of anti-cancer agents.Results: Chemotherapeutic cancer drugs were applied with or without nanoparticles to the skin of hairless mice, and their ability to penetrate the skin was assessed using fluorescence microscopy and tumor growth. Nanoparticles enhanced the penetration of the skin by doxorubicin and 5-fluorouracil as determined by fluorescence microscopy and growth retardation of experimental melanoma in immunocompetent, syngeneic mice. This drug enhancement did not require conjugation or encapsulation of the drugs by the nanoparticles – simple co-administration sufficed. Nanoparticles applied topically to melanomas increased the cytotoxicity and immune cell infiltration induced by co-administered 5-fluorouracil, and also reduced vascularization of the tumors independently of 5-fluorouracil.Conclusion: Correctly formulated superparamagnetic iron oxide nanoparticles can facilitate the chemotherapeutic effectiveness of cytotoxic drugs on skin tumors by both increasing their transdermal penetration and ameliorating host-tumor interactions. This enhancement of skin penetration occurs without the need for conjugation or encapsulation of the co-administered drugs and so will likely be applicable to other drugs, also.


1984 ◽  
Vol 17 (2) ◽  
pp. 89-93 ◽  
Author(s):  
Thaisa de Almeida Maria ◽  
Leny de Sousa Filardi ◽  
Zigman Brener

An electron microscopy study shows that the administration of a single dose (500 mg/kg, p.o.) of 2-amino-5-(1-methyl-5-nitro-2-imidazolyl)-1, 3, 4-thiadiazole induces in mice infected with Trypanosoma cruzi results in degenerative lesions of the intracellular stages. Ultrastructural alterations are detected as early as 6 hours after the drug administration and destruction of the parasites occurs within 18 - 36 hours. Trypomastigotes are cleared from the bloodstream 4 to 6 hours after treatment. The combined effect on both developmental stages is apparently responsible for the in vivo ejfects of this drug which is the most active drug ever tested in our laboratory in experimental Chagas' disease.


1993 ◽  
Vol 34 (2) ◽  
pp. 168-173
Author(s):  
Barry Högström ◽  
P. Rooth ◽  
O. Sunnegårdh ◽  
S.-O. Hietala

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