Effects of free and liposomized praziquantel on the surface morphology and motility of Mesocestoides vogae tetrathyridia (syn. M. corti ; Cestoda: Cyclophyllidea) in vitro

1998 ◽  
Vol 84 (3) ◽  
pp. 230-238 ◽  
Author(s):  
Gabriela Hrčková ◽  
Samuel Velebný ◽  
Julius Corba
Keyword(s):  
Surface Morphology ◽  
Mesocestoides Vogae

In Vivo and In Vitro Evaluation of Coated HAp Films with Different Surface Morphology

2007 ◽  
Vol 539-543 ◽  
pp. 710-715
Author(s):  
Kotaro Kuroda ◽  
Ryoichi Ichino ◽  
Masazumi Okido
Keyword(s):  
Bone Formation ◽  
Surface Morphology ◽  
New Bone Formation ◽  
Contact Ratio ◽  
Bone Implant ◽  
Ft Ir ◽  
Mouse Osteoblast ◽  
Surface Morphologies

Hydroxyapatite (HAp) coatings were formed on cp titanium plates and rods by the thermal substrate method in an aqueous solution that included 0.3 mM Ca(H2PO4)2 and 0.7 mM CaCl2. The coating experiments were conducted at 40-140 oC and pH = 8 for 15 or 30 min. The properties for the coated samples were studied using XRD, EDX, FT-IR, and SEM. All the specimens were covered with HAp, which had different surface morphologies such as net-like, plate-like and needle-like. After cleaning and sterilization, all the coated specimens were subjected to in vivo and vitro testing. In the in vitro testing, the mouse osteoblast-like cells (MC3T3-E1) were cultured on the coated and non-coated specimens for up to 30 days. Moreover, the specimens (φ2 x 5 mm) were implanted in rats femoral for up to 8 weeks, the osseoinductivity on them were evaluated. In in vitro evaluations, there were not significant differences between the different surface morphologies. In in vivo evaluations, however, two weeks postimplantation, new bone formed on both the HAp coated and non-coated titanium rods in the cancellous and cortical bone. The bone-implant contact ratio, which was used for the evaluation of new bone formation, was significantly dependent on the surface morphology of the HAp, and the results demonstrated that the needle-like coating appears to promote rapid bone formation.

Chitosan (Poly-(D) glucosamine) based solid lipid nanoparticles of dexibuprofen for topical delivery: Formulation development and characterizations

2021 ◽  
pp. 1-12
Author(s):  
Irshadullah ◽  
Shefaat Ullah Shah ◽  
Muhammad Khalid Khan ◽  
Kifayat Ullah Shah ◽  
Barkat Ali Khan
Keyword(s):  
Surface Morphology ◽  
Solid Lipid Nanoparticles ◽  
Active Drug ◽  
In Vitro Release ◽  
Topical Delivery ◽  
Lipid Nanoparticles ◽  
Solid Lipid ◽  
Permeation Study ◽  
Vitro Release

Chitosan a poly-(D) glucosamine is a polysaccharide made by treating shrimp and other crustacean shells with the alkali sodium hydroxide. It is a hydrophilic polymer that helps to retain the drug inside the solid lipid nanoparticles (SLN’s) and prolongs the release of drug from the carrier system. The purpose of the study was to formulate Chitosan decorated SLN’s for the topical delivery of dexibuprofen by hot pressure homogenization technique. Blank SLN’s, drug loaded SLN’s and Chitosan decorated SLN’s were prepared. Particle size, zeta potential and PDI were determined. FTIR study was conducted to evaluate the compatibility of excipients with the active drug. Surface morphology of SLN’s was determined by field emission scanning electron microscope. Drug content and entrapment efficiency of SLN’s were determined using indirect method. In vitro release and ex vivo permeation study of SLN’s were carried out using Franz diffusion cell. The droplet size fell into the nano range i.e. 132±7 to 424±2 nm which is effective for topical drug delivery system. The PDI of formulations range from 0.21 to 0.42 which depicts the homogeneity of all the SLN’s formulations. Vibrational analysis indicates that there is no interaction between active drug and excipient used in the formulation. The surface morphology revealed the spherical shape of Chitosan decorated SLN’s. The in vitro release of formulations showed 79.91±1.07 to 89.94±1.8 % drug release. The drug permeation study showed high permeation of drug into the skin. The percent drug permeation ranges from 64.15±0.93 to 71.80±0.88% indicating good permeation of drug across the skin. Overall, SLN’s are an effective carrier for topical delivery of dexibuprofen and thus bypasses side effects associated with oral delivery.

MORPHOLOGICAL, MICRO-MECHANICAL, CORROSION AND IN VITRO BIOACTIVITY INVESTIGATION OF SUPERFICIAL LAYER FORMATION DURING WIRE ELECTRICAL DISCHARGE MACHINING OF Ti-6Al-4V ALLOY FOR BIOMEDICAL APPLICATION

2021 ◽  
Author(s):  
SANDEEP MALIK ◽  
VINEET KUMAR
Keyword(s):  
Corrosion Resistance ◽  
Surface Morphology ◽  
Electrical Discharge ◽  
Electrical Discharge Machining ◽  
Biomedical Application ◽  
Superficial Layer ◽  
Pulse Interval ◽  
In Vitro Bioactivity ◽  
Nano Indentation

In this work, the experimental investigation of the surface integrity and biomechanical properties of the superficial layer obtained by wire electrical discharge machining (W-EDM) of Ti-6Al-4V alloy for biomedical application has been carried out. The surface morphology and elemental composition of the superficial layer have been investigated by field-emission scanning electron microscope (FE-SEM) and energy dispersive X-ray spectroscopy (EDS) techniques. The micro-mechanical behavior in terms of compressive strength and surface hardness was studied using the micro-pillar and nano-indentation technique. The corrosion resistance and in vitro bioactivity have been investigated using electrochemical and immersion test. Morphological analysis showed that surface morphology and superficial layer thickness were affected by peak current, pulse-duration and pulse-interval. The niobium (Nb)-rich layer was developed in superficial layer zone. The low peak current (3–6[Formula: see text]A), low pulse-duration (5–10[Formula: see text][Formula: see text]s) and high pulse-interval ([Formula: see text]s) have been recommended for better surface morphology and thin superficial layer (ranging from 4–6[Formula: see text][Formula: see text]m) free from surface defects. The micro-pillar and nano-indentation results showed that the superficial layer comprised of a brittle structure that improved the mechanical properties of the layer and the compressive strength was measured to be 1198 MPa. The corrosion resistance analysis revealed that the Nb-rich layer in the superficial layer improved the corrosion resistance and bioactivity. Excellent apatite growth has been found in the W-EDM-processed zone. The W-EDM can be used for the biomedical industry as a potential surface engineering technique.

Surface Structure and Cells Adhesion on Doped Polyethylene

2007 ◽  
Vol 567-568 ◽  
pp. 253-256
Author(s):  
Regina Mikulíková ◽  
Kateřina Kolářová ◽  
Václav Švorčík ◽  
Barbora Dvořánková ◽  
Tomáš Sopuch
Keyword(s):  
Surface Morphology ◽  
Ftir Spectroscopy ◽  
Crystalline Phase ◽  
Film Surface ◽  
Surface Wettability ◽  
Oxidized Cellulose ◽  
3T3 Fibroblasts ◽  
Doped Polymer

The properties of polyethylene doped with Ca2+ salt of oxidized cellulose was studied by different techniques. FTIR spectroscopy was used for the determination of crystalline phase in polymer film, surface wettability was determined by standard goniometry and surface morphology was examined by SEM microscopy. Adhesion of mouse 3T3 fibroblasts on the doped polymer was studied in vitro. It was found that the polyethylene doped with the cellulose derivative can be sterilized in boiling water. The number and homogeneity of adhering cells were shown to depend on the surface wettability and morphology.

scholarly journals EVALUATION OF STABILITY OF ROPINIROLE HYDROCHLORIDE AND PRAMIPEXOLE DIHYDROCHLORIDE MICROSPHERES AT ACCELERATED CONDITION

2018 ◽  
Vol 10 (4) ◽  
pp. 82
Author(s):  
Koyel Kar ◽  
R. N. Pal ◽  
Gouranga Nandi
Keyword(s):  
Particle Size ◽  
Drug Release ◽  
Surface Morphology ◽  
Shelf Life ◽  
Stability Study ◽  
In Vitro Drug Release ◽  
Drug Content ◽  
Ropinirole Hydrochloride ◽  
Pramipexole Dihydrochloride

Objective: The objective of the present work was to conduct accelerated stability study as per international council for harmonisation (ICH) guidelines and to establish shelf life of controlled release dosage form of ropinirole hydrochloride and pramipexole dihydrochloride microspheres for a period of 6 mo.Methods: Most optimized batch of ropinirole hydrochloride and pramipexole dihydrochloride (F12 and M12 respectively) were selected and subjected to exhaustive stability testing by keeping the sample in stability oven for a period of 3 and 6 mo. Various parameters like surface morphology, particle size, drug content, in vitro drug release and shelf life were evaluated at 3 and 6 mo period. The surface morphology of the formulated microspheres was determined by scanning electron microscopy (SEM). The particle size of the microspheres was estimated by optical microscopy method. The drug content was assayed by the help of ultra-violet spectrophotometer (UV). The in vitro drug release was performed by using Paddle II type dissolution apparatus and the filtrate was analyzed by UV spectrophotometer. The shelf life of the optimized microspheres was calculated by using the rate constant value of the zero-order reaction.Results: A minor change was recorded in average particle size of F12 and M12 microspheres after storage for 6 mo. For F12 and M12, initially the particle size was 130.00 µm and 128.92 µm respectively and after 6 mo it was found to be 130.92 µm and 128.99 µm respectively. There was no change in surface morphology of F12 and M12 microspheres after 6 mo of storage. The shape of microspheres remained spherical and smooth after 6 mo. An insignificant difference of drug content was recorded after 6 mo compared to the freshly prepared formulation. For F12 and M12, 94.50% and 93.77% of the drug was present initially and after 6 mo 94.45% and 93.72% of the drug was recorded. In vitro drug release was recorded after 6 mo for F12 and M12. Initially, 97.99% and 97.69% of the drug was released till 14th hour respectively for F12 and M12. After 6 mo, 98.23% and 97.99% of the drug was released respectively. The percentage residual drug content revealed that the degradation of microspheres was low. Considering the initial percentage residual drug content as 100%, 99.94% of the drug was recorded for both F12 and M12. The shelf life for F12 and M12 was found to be 10 y 52 d and 10 y 70 d respectively which were determined by the zero-order kinetic equation.Conclusion: A more or less similar surface morphology, particle size, drug content and percent of drug release before and after stability study confirmed the stability of F12 and M12 microspheres after storage for 6 mo and prove the efficacy of the microspheres in the site-specific delivery of drugs in Parkinson’s disease.

In vitro taurocholate-induced segmentation and clustering of Mesocestoides vogae (syn. corti) tetrathyridia (Cestoda) – inhibition by cestocidal drugs

2001 ◽  
Vol 87 (4) ◽  
pp. 281-286 ◽  
Author(s):  
Jenny Saldaña ◽  
Mónica Marín ◽  
Cecilia Fernández ◽  
Laura Domínguez
Keyword(s):  
Mesocestoides Vogae
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