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1.
AAPS PharmSciTech ; 23(3): 78, 2022 Feb 22.
Article in English | MEDLINE | ID: mdl-35194702

ABSTRACT

The patient-centric strategy urges the pharmaceutical companies to develop orodispersible films (ODF) as a new approach for pediatrics. However, the most common ODF-fabricated method, solvent casting, is facing the safety challenges of safety during manufacturing. To obtain favorable formulations with the ease of use and rapid dissolution, nanotechnology has been accounted for the development process. In this work, we investigated the wet-milling technique in preparing nanocarriers for loratadine-a hydrophobic anti-histamine drug. The results showed that the wet-milling technique could produce nanocarriers at the size of 400 nm. The reduction of particle size induced the increase of solubility and the dissolution rate of loratadine. Moreover, the pre-formulation of nanosized materials could adapt to the preparation of orodispersible films that disintegrated (less than 60s) and dissolved quickly. The DSC results showed that after the milling process, the crystallinity of loratadine was unchanged; however, the reduction in size induced an enhancement of drug bioavailability. After orally administrated to rats, the drug was quickly reached to the blood circulation, just after 30 min. Cmax increased from 44.97 ng/mL for the raw drug to 101.02 ng/mL for the nanocrystal leading to an enhancement of the AUC0-24h by 5.69-fold when the nanocrystal ODF was administrated. The ease of formulation and the improvement of drug solubility as well as bioavailability potentiated orodispersible films as a promising drug delivery for loratadine. Graphical abstract.


Subject(s)
Loratadine , Administration, Oral , Animals , Biological Availability , Child , Humans , Loratadine/chemistry , Particle Size , Rats , Solubility
2.
Stem Cell Rev Rep ; 17(6): 2291-2303, 2021 12.
Article in English | MEDLINE | ID: mdl-34510358

ABSTRACT

BACKGROUND: We have observed an increased expression of negative markers in some clinical-grade, xeno- and serum-free cultured adipose-derived mesenchymal stem/stromal cell (ADMSC) samples. It gave rise to concern that xeno- and serum-free conditions might have unexpected effects on human ADMSCs. This study aims to test this hypothesis for two xeno- and serum-free media, PowerStem MSC1 media (PS) and StemMACS MSC Expansion Media (SM), that support the in vitro expansion of ADMSCs. METHODS: We investigated the expression of negative markers in 42 clinical-grade ADMSC samples expanded in PS. Next, we cultured ADMSCs from seven donors in PS and SM and examined their growth and colony-forming ability, surface marker expression, differentiation, cell cycle and senescence, as well as genetic stability of two passages representing an early and late passage for therapeutic MSCs. RESULTS: 15 of 42 clinical-grade PS-expanded ADMSC samples showed an increased expression of negative markers ranging from 2.73% to 34.24%, which positively correlated with the age of donors. This rise of negative markers was related to an upregulation of Human Leukocyte Antigen - DR (HLA-DR). In addition, the PS-cultured cells presented decreased growth ability, lower frequencies of cells in S/G2/M phases, and increased ß-galactosidase activity in passage 7 suggesting their senescent feature compared to those grown in SM. Although MSCs of both PS and SM cultures were capable of multilineage differentiation, the PS-cultured cells demonstrated chromosomal abnormalities in passage 7 compared to the normal karyotype of their SM counterparts. CONCLUSIONS: These findings suggest that the SM media is more suitable for the expansion of therapeutic ADMSCs than PS. The study also hints a change of ADMSC features at more advanced passages and with increased donor's age. Thus, it emphasizes the necessity to cover these aspects in the quality control of therapeutic MSC products.


Subject(s)
HLA-DR Antigens , Mesenchymal Stem Cells , Cell Differentiation/genetics , Cell Proliferation/genetics , Culture Media, Serum-Free/metabolism , Culture Media, Serum-Free/pharmacology , HLA-DR Antigens/metabolism , Humans
3.
RSC Adv ; 11(50): 31641-31649, 2021 Sep 21.
Article in English | MEDLINE | ID: mdl-35496888

ABSTRACT

Desalination by solar steam generation (SSG) system is a green technology to produce pure water, which can address the issue of water scarcity. A novel photothermal material for the SSG system was fabricated by immersing bacterial cellulose (BC) sequentially into tannic acid (TA) and iron(iii) (Fe3+) solutions. Surface analysis of the resulting BC-TA-Fe3+ (BTF) material showed that coordination nanocomplexes between Fe3+ and hydroxyl groups of TA were formed on the surface of cellulose nanofibers. BTF material exhibited high sunlight absorption (∼95%), hydrophilic, self-cleaning properties, and excellent structural stability. SSG systems based on BTF had an evaporation efficiency of 91% and an evaporation rate of 1.56 kg m-2 h-1 under 1 sun illumination. Then, an efficient desalination device based on the larger-scale BTF material was fabricated to produce freshwater, the amount of freshwater per day was 5.6 kg m-2 on a sunny day. BTF material, thus, showed great potential in seawater desalination applications along with simple, versatile, scalable, and affordable fabrication methods.

4.
Cytotherapy ; 23(1): 88-99, 2021 01.
Article in English | MEDLINE | ID: mdl-33097415

ABSTRACT

BACKGROUND AIMS: Mesenchymal stem/stromal cells (MSCs) are of interest for the treatment of graft-versus-host disease, autoimmune diseases, osteoarthritis and neurological and cardiovascular diseases. Increasing numbers of clinical trials emphasize the need for standardized manufacturing of these cells. However, many challenges related to diverse isolation and expansion protocols and differences in cell tissue sources exist. As a result, the cell products used in numerous trials vary greatly in characteristics and potency. METHODS: The authors have established a standardized culture platform using xeno- and serum-free commercial media for expansion of MSCs derived from umbilical cord (UC), bone marrow and adipose-derived (AD) and examined their functional characteristics. RESULTS: MSCs from the tested sources stably expanded in vitro and retained their biomarker expression and normal karyotype at early and later passages and after cryopreservation. MSCs were capable of colony formation and successfully differentiated into osteogenic, adipogenic and chondrogenic lineages. Pilot expansion of UC-MSCs and AD-MSCs to clinical scale revealed that the cells met the required quality standard for therapeutic applications. CONCLUSIONS: The authors' data suggest that xeno- and serum-free culture conditions are suitable for large-scale expansion and enable comparative study of MSCs of different origins. This is of importance for therapeutic purposes, especially because of the numerous variations in pre-clinical and clinical protocols for MSC-based products.


Subject(s)
Cell Culture Techniques/instrumentation , Culture Media, Serum-Free/pharmacology , Mesenchymal Stem Cells/physiology , Adipogenesis , Adipose Tissue , Adult , Bone Marrow , Cell Differentiation , Cell Proliferation , Cells, Cultured , Chondrogenesis , Culture Media, Serum-Free/metabolism , Humans , Osteogenesis , Umbilical Cord
5.
Gene ; 513(1): 31-5, 2013 Jan 15.
Article in English | MEDLINE | ID: mdl-23142383

ABSTRACT

Type 2 diabetes (T2D) is a complex disorder resulting from both genetic and environmental factors in its pathogenesis. A case-control study was designed with subjects recruited from a general population to investigate whether the association between T2D and the common T>A polymorphism (rs9939609) in fat mass and obesity associated (FTO) gene is mediated by obesity-related measurements, considering the contribution of socio-economic status and lifestyle factors. The significant association between the FTO rs9939609 polymorphism and T2D was first observed in the model unadjusted (OR per A allele=1.61, 95% CI=1.06-2.44, P=0.024). It remained consistently replicated in the final model after adjustments for sex, age, systolic blood pressure, socio-economic status, lifestyle factors, and obesity-related measurements (body mass index, waist-hip ratio, body fat percentage, and body adiposity index), showing an increased T2D risk with an additive effect of the alleles (ORs per A allele=1.80-1.92, 95% CI=1.09-3.19, P<0.05). The FTO-rs9939609 polymorphism, systolic blood pressure, and waist-hip ratio were the most significant independent predictors for T2D, in which the power of the adjusted prediction model was 0.769. In conclusion, the study suggested that the FTO-rs9939609 polymorphism was significantly associated with the increased risk of T2D, independent of obesity-related measurements in a Vietnamese population.


Subject(s)
Asian People/genetics , Diabetes Mellitus, Type 2/genetics , Genetic Association Studies , Obesity/genetics , Polymorphism, Genetic , Proteins/genetics , Adiposity/genetics , Alpha-Ketoglutarate-Dependent Dioxygenase FTO , Case-Control Studies , Female , Genetic Predisposition to Disease , Humans , Life Style , Male , Middle Aged , Models, Genetic , Polymorphism, Single Nucleotide , Social Class , Vietnam
6.
AIDS Res Ther ; 9(1): 24, 2012 Aug 16.
Article in English | MEDLINE | ID: mdl-22897817

ABSTRACT

OBJECTIVE: This study reports the clinical characteristics and outcome of HIV-associated Penicilliummarneffei infection in northern Vietnam. METHODS: We conducted a retrospective chart review of all patients with laboratory confirmed Penicilliummarneffei infection admitted to the National Hospital for Tropical Diseases in Hanoi, Vietnam, between July 2006 and September 2009. RESULTS: 127 patients with P. marneffei infection were identified. All were HIV-infected; median CD4+ T-cell count was 24 cells/µl (IQR:12-48); 76% were men. Common clinical features were fever (92.9%), skin lesions (82.6%), hepatomegaly (61.4%), lymphadenopathy (40.2%), weight loss (59.1%) and cough (49.6%). Concurrent opportunistic infections were present in 22.0%; half of those had tuberculosis. Initial treatment regimens were: itraconazole or ketoconazole capsule (77.2%), amphotericin B (20.5%), and fluconazole (1.6%). In-hospital mortality was 12.6% and showed no significant difference in patients treated with itraconazole (or ketoconazole) and amphotericin B (p = 0.43). Dyspnea, ascites, and increased LDH level were independent predictors of mortality. No seasonality was observed. CONCLUSION: The clinical features, treatments and outcomes of HIV-associated P. marneffei infection in northern Vietnam are similar to those reported in other endemic regions. Dyspnea was an important predictor of mortality. More patients were treated with itraconazole than amphotericin B and no significant difference in treatment outcome was observed. It would be of clinical value to compare the efficacy of oral itraconazole and amphotericin B in a clinical trial.

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