Solidification of Nanostructured Lipid Carriers Loaded Testosterone Undecanoate: In Vivo and In Vitro Study

Drug Research ◽  
2018 ◽  
Vol 68 (08) ◽  
pp. 457-464
Author(s):  
Yabing Hua ◽  
Wanqing Li ◽  
Zhou Cheng ◽  
Ziming Zhao ◽  
Xiaoxing Yin ◽  
...  
Keyword(s):  
In Vitro Study ◽  
Cell Permeability ◽  
Vacuum System ◽  
Protective Agent ◽  
Scanning Calorimetry ◽  
Testosterone Undecanoate ◽  
Transmission Electron ◽  
Dissolution In Vitro

To enhance the bioavailability of testosterone undecanoate (TU) and overcome the current problem of soft capsules (Andriol Testocaps®), Nano-structured lipid carriers (NLC) for TU was developed. First, suspension of TU-loaded NLC (TU-NLC) was prepared by high pressure homogenization; then adsorbent or a protective agent β-cyclodextrin was used to solidify the suspension through a vacuum system; finally, the solid powder of TU-loaded NLC (solid TU-NLC) was filled into hard capsules. The characteristics of solid TU-NLC, were investigated in vitro and vivo. The particle size of TU-NLC was about 273.3 nm, the potential was 0.156±0.04. Transmission electron microscope (TEM) revealed that the NLC was spherical and uniform. Differential scanning calorimetry (DSC) suggested the drug had been encapsulated into NLC lipid matrix. The drug release proved that solid TU-NLC showed a higher dissolution in vitro. The CaCO-2 cell permeability showed that solid TU-NLC could enhance trans-membrane absorption of the TU. Moreover, the AUC of solid TU-NLC formulations (4304±550.50 μg/L*min) was higher than commercial product Andriol Testocaps® (3075±372.50 μg/L*min). In conclusion, solid TU-NLC could enhance the rate of dissolution, and had a relatively higher bioavailability than Andriol Testocaps® in vivo Graphical Abstract.

Design, technological development and evaluation of stimuli-responsive chimeric nanocarriers for cancer therapy

2019 ◽  
Author(s):  
Νικόλαος Ναζίρης
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Technological Development ◽  
Stimuli Responsive ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Micro Dsc

Η επιστήμη έχει σημαντικά επιτεύγματα μέσω της Νανοτεχνολογίας, με εφαρμογές οι οποίες ξεπερνούν κατά πολύ τις δυνατότητες των συμβατικών μέσων σε πολλά επιστημονικά πεδία, συμπεριλαμβανομένης της Ιατρικής και της Φαρμακευτικής. Η Νανοϊατρική ευδοκιμεί μετά την ανάπτυξη των πρώτων νανοτεχνολογικών φαρμάκων στα τέλη του 20ου αιώνα και αναπτύχθηκε ώστε να αποτελεί μία από τις πιο υποσχόμενες προσπάθειες στον αγώνα κατά των ανθρωπίνων ασθενειών. Σε αυτό το πλαίσιο, τα λιποσώματα από καιρού αξιοποιούνται ως νανοτεχνολογικοί φορείς φαρμακομορίων και θεωρούνται ως μία από τις πιο καλώς μελετημένες πλατφόρμες για αυτόν τον σκοπό. Αυτοί οι νανοφορείς ομοιάζουν με τα κύτταρα και χαρακτηρίζονται από δομή και ιδιότητες στη μεσοκλίμακα τα οποία είναι δυναμικά, κυριαρχούμενα από το μηχανισμό και τους νόμους που διέπουν την αυτο-συναρμολόγηση. Η διαδικασία αυτή φέρει κρίσιμη σημασία για την ανάπτυξη νέων και καινοτόμων φαρμακευτικών προϊόντων, όπως και για τη νομοθετική ρύθμιση των ακολούθων “νανο-ομοειδών” φαρμάκων.Η παρούσα διδακτορική διατριβή πραγματεύεται το σύγχρονο θέμα των αποκρινόμενων σε ερεθίσματα χιμαιρικών/μικτών νανοφορέων για τη θεραπεία του καρκίνου, οι οποίοι ανήκουν στην τάξη των καινοτόμων νανοσυστημάτων μεταφοράς φαρμακομορίων για πολύπλοκες ασθένειες. Σκοπός της έρευνας ήταν ο ορθολογικός σχεδιασμός και η ανάπτυξη χιμαιρικών νανοσυστημάτων, οι οποίοι θα αποκρίνονται σε συγκεκριμένες φυσικές και φυσιολογικές συνθήκες, όπως αλλαγές στη θερμοκρασία και μεταβολές του pH, αλλά και η αξιολόγηση της συμπεριφοράς τους κατά την αυτο-συναρμολόγηση, των τελικών ιδιοτήτων τους και της in vitro και in vivo δράσης τους. Αυτά τα νανοσυστήματα αποτελούνται από δύο διαφορετικές τάξεις βιοϋλικών, ήτοι φωσφολιπίδια και αμφίφιλα δισυσταδικά συμπολυμερή και είναι υποσχόμενοι φαρμακοφορείς για τη θεραπεία διαφόρων τύπων καρκίνου, μεταφέροντας και απελευθερώνοντας θεραπευτικούς παράγοντες επιλεκτικά στο σημείο της νόσου.Τα αναλυτικά εργαλεία τα οποία χρησιμοποιήθηκαν για την αξιολόγηση των αλληλεπιδράσεων μεταξύ των βιοϋλικών και της αυτο-συναρμολογήσεώς τους συνεισφέρουν στην ανάπτυξη ποιοτικών νανοτεχνολογικών σκευασμάτων, προσφέροντας γνώση επί των ιδιοτήτων στη νανοκλίμακα αυτών των συστημάτων και της σχέσεις τους με τον τελικό νανοφορέα. Τα εργαλεία αυτά σχετίζονται με τη θερμοδυναμική, τις φυσικοχημικές ιδιότητες, τη σταθερότητα, τη μορφολογία, τη βιοφυσική και τη λειτουργικότητα και τελικώς, με τη βιολογική τοξικότητα και αποτελεσματικότητα των χιμαιρικών νανοσυστημάτων. Συγκεκριμένα, αυτά περιλαμβάνουν τη θερμική ανάλυση, όπως είναι η διαφορική θερμιδομετρία σαρώσεως (differential scanning calorimetry, DSC) ή η micro-DSC, τη σκέδαση φωτός, τεχνικές απεικονίσεως, όπως είναι η ηλεκτρονική μικροσκοπία διαπερατότητας (transmission electron microscopy, TEM) και η κρυογονική ηλεκτρονική μικροσκοπία μεταδόσεως διαπερατότητας (cryogenic TEM, cryo-TEM) και τέλος, βιολογικές δοκιμασίες, μέσω in vitro και in vivo μοντέλων. Ο πλήρης χαρακτηρισμός ενός νανοσυστήματος, όπως τα λιποσώματα, βάσει των εργαλείων αυτών, όχι μόνο συνδράμει στην ανάπτυξη καινοτόμων νανοσυστημάτων μεταφοράς φαρμακομορίων, αλλά και στην κατανόηση του ρόλου του κάθε μοριακού συστατικού του συστήματος και της διαδικασίας της αυτo-οργανώσεως στο τελικό φαρμακευτικό προϊόν.Τελικώς, η παρούσα διδακτορική έρευνα οδήγησε στην ανάπτυξη βιοσυμβατών και λειτουργικών χιμαιρικών νανοσυστημάτων, τα οποία είναι υποσχόμενα ως πλατφόρμες μεταφοράς φαρμακομορίων για καρκίνο, μέσω της αποκρινόμενης σε ερεθίσματα συμπεριφοράς τους. Η αξία της εγκαθιδρύσεως μιας λογικής για την αξιολόγηση των νανοσυστημάτων τέτοιου τύπου μέσω του συνδυασμού συγκεκριμένων και σημαντικών εργαλείων είναι επίσης εμφανής και θα προσφέρει γνώση για την περαιτέρω ανάπτυξη καινοτόμων φαρμάκων. Επιπλέον, θα συνδράμει και στη μελέτη και έγκριση των ακολούθων προϊόντων αυτών, τα οποία είναι γνωστά ως “νανο-ομοειδοί”. Τα εργαλεία αυτά αφορούν την αξιολόγηση του μηχανισμού της αυτο-συναρμολογήσεως και της σχέσης της με τις ιδιότητες, την τοξικότητα και τη λειτουργικότητα των καινοτόμων νανοσυστημάτων μεταφοράς φαρμακομορίων, με τελικό στόχο την ανάπτυξη ποιοτικών, ασφαλών και αποτελεσματικών καινοτόμων φαρμάκων για τη θεραπεία του καρκίνου.

scholarly journals pH-responsive delivery vehicle based on RGD-modified polydopamine-paclitaxel-loaded poly (3-hydroxybutyrate-co-3-hydroxyvalerate) nanoparticles for targeted therapy in hepatocellular carcinoma

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Mingfang Wu ◽  
Chen Zhong ◽  
Qian Zhang ◽  
Lu Wang ◽  
Lingling Wang ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Scanning Calorimetry ◽  
Anticancer Efficacy ◽  
Coated Nanoparticles ◽  
Transmission Electron ◽  
Sensitive Coating ◽  
Arginine Glycine Aspartic Acid ◽  
The Michael Addition

AbstractA limitation of current anticancer nanocarriers is the contradiction between multiple functions and favorable biocompatibility. Thus, we aimed to develop a compatible drug delivery system loaded with paclitaxel (PTX) for hepatocellular carcinoma (HCC) therapy. A basic backbone, PTX-loaded poly (3-hydroxybutyrate-co-3-hydroxyvalerate) PHBV nanoparticle (PHBV-PTX-NPs), was prepared by emulsion solvent evaporation. As a gatekeeper, the pH-sensitive coating was formed by self-polymerization of dopamine (PDA). The HCC-targeted arginine-glycine-aspartic acid (RGD)-peptide and PDA-coated nanoparticles (NPs) were combined through the Michael addition. Subsequently, the physicochemical properties of RGD-PDA-PHBV-PTX-NPs were characterized by dynamic light scattering-autosizer, transmission electron microscope, fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetry and X-ray spectroscopy. As expected, the RGD-PDA-PHBV-PTX-NPs showed robust anticancer efficacy in a xenograft mouse model. More importantly, they exhibited lower toxicity than PTX to normal hepatocytes and mouse in vitro and in vivo, respectively. Taken together, these results indicate that the RGD-PDA-PHBV-PTX-NPs are potentially beneficial for easing conflict between multifunction and biocompatible characters of nanocarriers.

scholarly journals Assessment of Antifungal Efficacy and Release Behavior of Fungicide-Loaded Chitosan-Carrageenan Nanoparticles against Phytopathogenic Fungi

Polymers ◽  
2021 ◽  
Vol 14 (1) ◽  
pp. 41
Author(s):  
Ravinder Kumar ◽  
Agnieszka Najda ◽  
Joginder Singh Duhan ◽  
Balvinder Kumar ◽  
Prince Chawla ◽  
...  
Keyword(s):  
Growth Parameters ◽  
In Vitro Study ◽  
Alternaria Solani ◽  
Germination Percentage ◽  
Phytopathogenic Fungi ◽  
Release Behavior ◽  
Scanning Calorimetry ◽  
Root Shoot Ratio

Biopolymeric Chitosan-Carrageenan nanocomposites 66.6–231.82 nm in size containing the chemical fungicide mancozeb (nano CSCRG-M) were synthesized following a green chemistry approach. The physicochemical study of nanoparticles (NPs) was accomplished using a particle size analyzer, SEM and FTIR. TEM exhibited clover leaf-shaped nanoparticles (248.23 nm) with mancozeb on the inside and entrapped outside. Differential scanning calorimetry and TGA thermogravimetry exhibited the thermal behaviour of the nanoform. Nano CSCRG-1.5 at 1.5 ppm exhibited 83.1% inhibition against Alternaria solani in an in vitro study and performed as well as mancozeb (84.6%). Complete inhibition was exhibited in Sclerotinia sclerotiorum at 1.0 and 1.5 ppm with the nanoformulation. The in vivo disease control efficacy of mancozeb-loaded nanoparticles against A. solani in pathogenized plants was found to be relatively higher (79.4 ± 1.7) than that of commercial fungicide (76 ± 1.1%) in pot conditions. Nanomancozeb showed superior efficacy for plant growth parameters, such as germination percentage, root–shoot ratio and dry biomass. The nanoformulation showed higher cell viability compared to mancozeb in Vero cell cultures at 0.25 and 0.50 mg/mL in the resazurin assay. CSCRG-0.5 showed slow-release behavior up to 10 h. Thus, these green nano-based approaches may help combat soil and water pollution caused by harmful chemical pesticides.

scholarly journals Nanocarriers From Natural Lipids With In Vitro Activity Against Campylobacter jejuni

2021 ◽  
Vol 10 ◽  
Author(s):  
Lígia Nunes de Morais Ribeiro ◽  
Eneida de Paula ◽  
Daise Aparecida Rossi ◽  
Flávia Alves Martins ◽  
Roberta Torres de Melo ◽  
...  
Keyword(s):  
Campylobacter Jejuni ◽  
Vegetable Oils ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Vero Cell Line ◽  
Physicochemical Stability ◽  
Nanoparticle Morphology ◽  
Dsc Analyses

Campylobacter jejuni (CJ) is the most prevalent zoonotic pathogen of chicken meat and related products, which may lead to gastroenteritis and autoimmune diseases in humans. Although controlling this bacterium is important, CJ strains resistance against traditional antibiotic therapy has been increased. Vegetable oils and fats are natural biomaterials explored since the Ancient times, due to their therapeutic properties. Nanotechnology has promoted the miniaturization of materials, improving bioavailability and efficacy, while reducing the toxicity of loaded active molecules. In this work, a screening of 28 vegetable oils was firstly performed, in order to select anti-CJ candidates by the disc diffusion test. Thus, the selected liquid lipids were used as active molecules in nanostructured lipid carriers (NLC) formulations. The three resultant systems were characterized in terms of particle size (~200 nm), polydispersity index (~0.15), and zeta potential (~-35mV), and its physicochemical stability was confirmed for a year, at 25°C. The structural properties of NLC were assessed by infrared (FTIR-ATR) and differential scanning calorimetry (DSC) analyses. The spherical nanoparticle morphology and narrow size distribution was observed by transmission electron microscopy (TEM) and field emission scanning electron (FE-SEM) analyses, respectively. Then, the in vitro antimicrobial activity test determined the minimum inhibitory concentration (MIC) of each formulation against CJ strains, in both free (1–3 mg/ml−1) and sessile (0.78 mg/ml−1) forms. Finally, the in vitro biocompatibility of NLC was demonstrated through cell viability using VERO cell line, in which F6 was found twice less cytotoxic than pure olibanum oil. Considering the abovementioned achieved, F6 formulation is able to be evaluated in the in vivo anti-CJ efficacy assays.

Formulation, Characterization and In-vitro and In-vivo Evaluation of Capecitabine Loaded Niosomes

2020 ◽  
Vol 17 (3) ◽  
pp. 257-268
Author(s):  
Parth Patel ◽  
Tejas Barot ◽  
Pratik Kulkarni
Keyword(s):  
Particle Size ◽  
Entrapment Efficiency ◽  
Particle Size Analysis ◽  
Multi Drug Resistance ◽  
Size Analysis ◽  
Scanning Calorimetry ◽  
In Vivo Evaluation ◽  
Transmission Electron

Background: Nanocarriers improve the efficacy of drugs by facilitating their specific delivery and protecting them from external environment resulting in a better performance against diseases. Objective: In this study, it was aimed to improve the efficacy of capecitabine against colorectal cancer by its entrapment in niosomes. Ether injection method was used to prepare niosomes composed of span 20 and cholesterol. Methods: Niosomes were evaluated by evaluating the entrapment efficiency, in-vitro drug release and cytotoxicity of capecitabine loaded niosomes. Niosomes were characterized by particle size analysis, transmission electron microscopy, Fourier transform infrared spectroscopy and differential scanning calorimetry for surface morphology and drug excipient interactions. Results: High encapsulation efficiency (90.55%) was observed, which is anticipated to resolve the multi-drug resistance problem. Reported particle size was 180.9 + 5 nm with a negative zeta potential - 21 + 0.5 mV and the kinetic study showed a concentration-dependent release of the drug from the niosome. DSC study proved entrapment of the entire drug and its non-covalent bonding with the excipients. Cytotoxicity study of niosomes on CaCO2 cell line showed an improved IC>50 value as compared to the free drug. Conclusion: Enhanced cytotoxicity observed in the results further supports the suitability of niosome as a nanocarrier for pharmaceutical drug delivery.

Effects of TSH and calcitriol on bone metabolism: in vivo and in vitro study

2014 ◽  
Author(s):  
Ivo Dumic-Cule ◽  
Dunja Rogic ◽  
Damir Jezek ◽  
Lovorka Grgurevic ◽  
Slobodan Vukicevic
Keyword(s):  
Bone Metabolism ◽  
In Vitro Study ◽  
Vitro Study

Fenofibrate Solid Dispersion for Improving Oral Bioavailability: Preparation, and Characterization and in vivo Evaluation

2020 ◽  
Vol 13 (5) ◽  
pp. 5102-5109
Author(s):  
Venu Madhav K ◽  
Somnath De ◽  
Chandra Shekar Bonagiri ◽  
Sridhar Babu Gummadi
Keyword(s):  
Oral Bioavailability ◽  
Oral Delivery ◽  
Solid Dispersions ◽  
In Vitro Release ◽  
Aqueous Solubility ◽  
Water Soluble ◽  
Scanning Calorimetry ◽  
In Vivo Evaluation

Fenofibrate (FN) is used in the treatment of hypercholesterolemia. It shows poor dissolution and poor oral bioavailability after oral administration due to high liphophilicity and low aqueous solubility. Hence, solid dispersions (SDs) of FN (FN-SDs) were develop that might enhance the dissolution and subsequently oral bioavailability. FN-SDs were prepared by solvent casting method using different carriers (PEG 4000, PEG 6000, β cyclodextrin and HP β cyclodextrin) in different proportions (0.25%, 0.5%, 0.75% and 1% w/v). FN-SDs were evaluated solubility, assay and in vitro release studies for the optimization of SD formulation. Differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD) and scanning electron microscopy (SEM) analysis was performed for crystalline and morphology analysis, respectively. Further, optimized FN-SD formulation evaluated for pharmacokinetic performance in Wistar rats, in vivo in comparison with FN suspension.  From the results, FN-SD3 and FN-SD6 have showed 102.9 ±1.3% and 105.5±3.1% drug release, respectively in 2 h. DSC and PXRD studies revealed that conversion of crystalline to amorphous nature of FN from FT-SD formulation. SEM studies revealed the change in the orientation of FN when incorporated in SDs. The oral bioavailability FN-SD3 and FN-SD6 formulations exhibited 2.5-folds and 3.1-folds improvement when compared to FN suspension as control. Overall, SD of FN could be considered as an alternative dosage form for the enhancement of oral delivery of poorly water-soluble FN.

Pharmacokinetic Evaluation of 99mTc-radiolabeled Solid Lipid Nanoparticles and Chitosan Coated Solid Lipid Nanoparticles

2020 ◽  
Vol 20 (13) ◽  
pp. 1044-1052
Author(s):  
Nasrin Abbasi Gharibkandi ◽  
Sajjad Molavipordanjani ◽  
Jafar Akbari ◽  
Seyed Jalal Hosseinimehr
Keyword(s):  
Solid Lipid Nanoparticles ◽  
Lipid Nanoparticles ◽  
High Resistivity ◽  
Scanning Calorimetry ◽  
Liver Uptake ◽  
Solid Lipid ◽  
Transmission Electron ◽  
Main Portion ◽  
Pharmacokinetic Behavior

Background: Solid Lipid Nanoparticles (SLNs) possess unique in vivo features such as high resistivity, bioavailability, and habitation at the target site. Coating nanoparticles with polymers such as chitosan greatly affects their pharmacokinetic behavior, stability, tissue uptake, and controlled drug delivery. The aim of this study was to prepare and evaluate the biodistribution of 99mTc-labeled SLNs and chitosan modified SLNs in mice. Methods: 99mTc-oxine was prepared and utilized to radiolabel pre-papered SLNs or chitosan coated SLNs. After purification of radiolabeled SLNs (99mTc-SLNs) and radiolabeled chitosan-coated SLNs (99mTc-Chi-SLNs) using Amicon filter, they were injected into BALB/c mice to evaluate their biodistribution patterns. In addition, nanoparticles were characterized using Transmission Electron Microscopy (TEM), Fourier-transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), X-ray Powder Diffraction (XRD) and Dynamic Light Scattering (DLS). Results: 99mTc-oxine with high radiochemical purity (RCP~100%) and stability (RCP > 97% at 24 h) was used to provide 99mTc-SLNs and 99mTc-Chi-SLNs with high initial RCP (100%). TEM image and DLS data suggest 99mTc- SLNs susceptibility to aggregation. To that end, the main portion of 99mTc-SLNs radioactivity accumulates in the liver and intestines, while 99mTc-Chi-SLNs sequesters in the liver, intestines and kidneys. The blood radioactivity of 99mTc-Chi-SLNs was higher than that of 99mTc-SLNs by 7.5, 3.17 and 3.5 folds at 1, 4 and 8 h post-injection. 99mTc- Chi-SLNs uptake in the kidneys in comparison with 99mTc-SLNs was higher by 37.48, 5.84 and 11 folds at 1, 4 and 8h. Conclusion: The chitosan layer on the surface of 99mTc-Chi-SLNs reduces lipophilicity in comparison with 99mTc- SLNs. Therefore, 99mTc-Chi-SLNs are less susceptible to aggregation, which leads to their lower liver uptake and higher kidney uptake and blood concentration.

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