Amniotic membrane as a scaffold in wound healing and diabetic foot ulcer: an experimental technique and recommendations

Background: Human amniotic membrane has been used clinically in a variety of applications for over the past 100 years and produced a significant amount of data in multiple areas of medicine. Its clinical usage ranges from wound coverage for burn victims to healing of the conjunctiva after pterygium repair. The amniotic membrane natural properties provide an easy to use, safe option for various medical applications. There is need to develop a method for storage of amniotic membrane which can retain the biological properties and as well have long shelf life too.Methods: The experimental technique was standardized for cryopreservation of amniotic membrane. For this, amniotic membrane was obtained from mothers who had delivered through caesarean section with their consent.Results: The standardized protocol for cryopreservation of amniotic membrane was found to be safe and preserved amniotic membrane is expected to have long shelf life.  Conclusions: The advantages associated with amniotic membrane such as easily available, inexpensive, non-immunogenic and antimicrobial, anti-inflammatory properties make it a suitable graft to be used in wound healing and diabetic foot ulcers

Desarrollo y validación de un método por cromatografía líquida de alta resolución para la estimación de esomeprazol en forma de dosificación a granel y en tableta

Introduction: An accurate, simple, precise, rapid, economic and reproducible reverse-phase high-performance liquid chromatography method was developed and validated for the estimation of Esomeprazole (ESO) in bulk and tablet dosage form. Method: The separation was carried out on Finepak SIL C18T-5 column (250 × 4.6 mm, 5.0 µm i. d.) using potassium dihydrogen phosphate buffer (0.025M): ACN (20:80 v/v) and at a flow rate of 1.0 mL/min. using UV detector at 302 nm with a run time of 10 min. The method was validated for accuracy for linearity, accuracy, precision, limit of detection (LOD), limit of quantification (LOQ) and robustness. Results: The standard calibration curve was linear with R2 = 0.995. LOD and LOQ obtained for esomeprazole were 0.0001 and 0.0004 µg/mL respectively. The method was found robust for possible changes. Results of analysis of other parameters were also tested and validated as per ICH guidelines and recovery studies confirmed the accuracy of the proposed method. validation studies showed that the developed HPLC method is simple, reproducible, rapid, precise and reliable. The high recovery and low relative standard deviation confirm the suitability of the developed method for the determination of esomeprazole in the tablet dosage form. Conclusion: This method may be used as a more convenient and efficient option for the analysis of esomeprazole to establish the quality of the substance during routine analysis with consistent and reproducible results.Introducción: Se desarrolló y validó un método de cromatografía líquida de alta resolución de fase reversa exacto, simple, preciso, rápido, económico y reproducible para la estimación de esomeprazol (ESO) en forma de dosificación a granel y en tabletas. Método: La separación se llevó a cabo en columna Finepak SIL C18T-5 (250 × 4,6 mm; 5,0 µm i.d.) utilizando tampón fosfato dihidrógeno de potasio (0,025 M): ACN (20:80 v/v) y a un caudal de 1,0 ml/min. utilizando un detector UV a 302 nm con un tiempo de ejecución de 10 min. El método fue validado para exactitud de linealidad, exactitud, precisión, límite de detección (LOD), límite de cuantificación (LOQ) y robustez. Resultados: La curva de calibración estándar fue lineal con R2 = 0,995. El LOD y el LOQ obtenidos para esomeprazol fueron 0,0001 y 0,0004 µg/mL respectivamente. El método se encontró robusto para posibles cambios. Los resultados del análisis de otros parámetros también se probaron y validaron según las pautas de ICH y los estudios de recuperación confirmaron la precisión del método propuesto. Los estudios de validación mostraron que el método HPLC desarrollado es simple, reproducible, rápido, preciso y confiable. La alta recuperación y la baja desviación estándar relativa confirman la idoneidad del método desarrollado para la determinación de esomeprazol en forma de dosificación en tabletas. Conclusión: Este método puede ser utilizado como una opción más conveniente y eficiente para el análisis de esomeprazol para establecer la calidad de la sustancia durante el análisis de rutina con resultados consistentes y reproducibles

A Review on Physical, Chemical and Optical Properties of Liquid Crystal

The foundation of the upcoming generation of cutting-edge gadgets and digitally augmented technologies is expected to be smart soft materials. Because of their responsiveness and adaptability, liquid crystals (LCs) are promising smart soft materials. In the 20th century, LCs were crucial to changing the information display sector. However, several beyond-display uses for LCs have been proven at the turn of the twentieth century, neatly using their controlled stimuli-responsive and adaptable properties. New LC materials have been developed and engineered for such applications. The review comes close with a summary and viewpoints on the potential and problems facing LCs as smart soft materials. This review is expected to inspire a wide range of concepts for the application of nature's delicate phase of matter in the generation and beyond of smart and augmented devices

Desarrollo y validación de un método por cromatografía líquida de alta resolución para la estimación de esomeprazol en forma de dosificación a granel y en tableta

The authors are thankful to JSPM’s Charak College of Pharmacy and Research, Pune for providing instrumental facilities and infrastructure for the successful completion of research workIntroduction: An accurate, simple, precise, rapid, economic and reproducible reverse-phase high-performance liquid chromatography method was developed and validated for the estimation of Esomeprazole (ESO) in bulk and tablet dosage form. Method: The separation was carried out on Finepak SIL C18T-5 column (250 × 4.6 mm, 5.0 µm i. d.) using potassium dihydrogen phosphate buffer (0.025M): ACN (20:80 v/v) and at a flow rate of 1.0 mL/min. using UV detector at 302 nm with a run time of 10 min. The method was validated for accuracy for linearity, accuracy, precision, limit of detection (LOD), limit of quantification (LOQ) and robustness. Results: The standard calibration curve was linear with R2 = 0.995. LOD and LOQ obtained for esomeprazole were 0.0001 and 0.0004 µg/mL respectively. The method was found robust for possible changes. Results of analysis of other parameters were also tested and validated as per ICH guidelines and recovery studies confirmed the accuracy of the proposed method. validation studies showed that the developed HPLC method is simple, reproducible, rapid, precise and reliable. The high recovery and low relative standard deviation confirm the suitability of the developed method for the determination of esomeprazole in the tablet dosage form. Conclusion: This method may be used as a more convenient and efficient option for the analysis of esomeprazole to establish the quality of the substance during routine analysis with consistent and reproducible results.Introducción: Se desarrolló y validó un método de cromatografía líquida de alta resolución de fase reversa exacto, simple, preciso, rápido, económico y reproducible para la estimación de esomeprazol (ESO) en forma de dosificación a granel y en tabletas. Método: La separación se llevó a cabo en columna Finepak SIL C18T-5 (250 × 4,6 mm; 5,0 µm i.d.) utilizando tampón fosfato dihidrógeno de potasio (0,025 M): ACN (20:80 v/v) y a un caudal de 1,0 ml/min. utilizando un detector UV a 302 nm con un tiempo de ejecución de 10 min. El método fue validado para exactitud de linealidad, exactitud, precisión, límite de detección (LOD), límite de cuantificación (LOQ) y robustez. Resultados: La curva de calibración estándar fue lineal con R2 = 0,995. El LOD y el LOQ obtenidos para esomeprazol fueron 0,0001 y 0,0004 µg/mL respectivamente. El método se encontró robusto para posibles cambios. Los resultados del análisis de otros parámetros también se probaron y validaron según las pautas de ICH y los estudios de recuperación confirmaron la precisión del método propuesto. Los estudios de validación mostraron que el método HPLC desarrollado es simple, reproducible, rápido, preciso y confiable. La alta recuperación y la baja desviación estándar relativa confirman la idoneidad del método desarrollado para la determinación de esomeprazol en forma de dosificación en tabletas. Conclusión: Este método puede ser utilizado como una opción más conveniente y eficiente para el análisis de esomeprazol para establecer la calidad de la sustancia durante el análisis de rutina con resultados consistentes y reproducibles

Electrospun Nanofibers of Conducting Polyaniline/Al-SnO2 Composites for Hydrogen Sensing Applications

AbstractIn this paper, we report the synthesis and characterization of composites of polyaniline and aluminum doped tin oxide (Al-SnO2/PANI) nanofibers for hydrogen gas sensing application. Al-SnO2/PANI composite nanofibers have been fabricated via electrospinning technique and subsequent calcination procedure. The as-prepared Al-SnO2/PANI composite nanofibers were investigated for structural characterizations by means of SEM, FTIR, UV-VIS and XRD. SEM revealed the nanofibers with the diameter around 200-300nm formed a non-woven material with highly porous and agglomerated structure. FTIR and UV-VIS spectra revealed the possible incorporation of Al-SnO2 in PANI and confirmed the uniform attachment of PANI on the surface of Al-SnO2 nanostructures. XRD showed peak broadening and the peak positions shift from standard values, indicating presence of aluminum doped tin oxide in nanoparticles form in the polyaniline (PANI) matrix. On exposure to hydrogen gas (1000ppm), it was found that the nanofibers of Al-SnO2/PANI composite showed high sensitivity at 48 oC with relatively faster response/recovery as compared to pure SnO2 and Al doped SnO2 nanofibers

Determinants of Chromosome Architecture: Insulator Pairing in cis and in trans.

The chromosomes of multicellular animals are organized into a series of topologically independent looped domains. This domain organization is critical for the proper utilization and propagation of the genetic information encoded by the chromosome. A special set of architectural elements, called boundaries or insulators, are responsible both for subdividing the chromatin into discrete domains and for determining the topological organization of these domains. Central to the architectural functions of insulators are homologous and heterologous insulator:insulator pairing interactions. The former (pairing between copies of the same insulator) dictates the process of homolog alignment and pairing in trans, while the latter (pairing between different insulators) defines the topology of looped domains in cis. To elucidate the principles governing these architectural functions, we use two insulators, Homie and Nhomie, that flank the Drosophila even skipped locus. We show that homologous insulator interactions in trans, between Homie on one homolog and Homie on the other, or between Nhomie on one homolog and Nhomie on the other, mediate transvection. Critically, these homologous insulator:insulator interactions are orientation-dependent. Consistent with a role in the alignment and pairing of homologs, self-pairing in trans is head-to-head. Head-to-head self-interactions in cis have been reported for other fly insulators, suggesting that this is a general principle of self-pairing. Homie and Nhomie not only pair with themselves, but with each other. Heterologous Homie-Nhomie interactions occur in cis, and we show that they serve to delimit a looped chromosomal domain that contains the even skipped transcription unit and its associated enhancers. The topology of this loop is defined by the heterologous pairing properties of Homie and Nhomie. Instead of being head-to-head, which would generate a circular loop, Homie-Nhomie pairing is head-to-tail. Head-to-tail pairing in cis generates a stem-loop, a configuration much like that observed in classical lampbrush chromosomes. These pairing principles provide a mechanistic underpinning for the observed topologies within and between chromosomes

Observational study of victims of alleged sexual assault in central Mumbai region

According to recent, Criminal Law (Amendment) Act 2013, age of consent in India has been increased from 16 to 18 years. Implications of the amendments made, are vastly reflected in data collected in our study. Aim of the study was to evaluate data in relation to incidences of alleged sexually abused victims and to contemplate their socio demographic profile with history and examination and also to assess the effect of increase in age of consent for sexual intercourse. This study was conducted on 58 cases of alleged sexual assault brought to Seth G.S. Medical College, K.E.M. Hospital, Mumbai, from September 2013 to February 2015. Out of 58 victims of alleged sexual assault, the most affected age group was 10-19 years i.e. 34 cases (58.62 %), while 18 cases (31.03%) were in the age group of 16-18 years. The highest number of victims 18 (31.03 %) were brought for examination more than three weeks after incident resulting in loss of vital trace evidences. 58.62% of victims knew the assailant. In consensual relationships, breach of trust resulted in complaint of sexual assault, thus crime was registered under Section 375 IPC. Our study critically analyzes entailments of Criminal law amendment act, 2013; in relation to the data collected. Reductions in age of consent, in order to protect rights of young persons aged 16-18 years to engage in consensual sexual activity should be deliberated.</p

Biological and synthetic scaffold: an extra cellular matrix for constructive tissue engineering

Worldwide many people suffering from tissue dysfunctions or damages need rapid transplantation. Tissue engineering has attracted attention as therapeutic modality aiming at repairing lost or damaged tissues. Critical step in tissue engineering is fabrication of three dimensional scaffolds which mimic the extracellular matrix of tissues and promote tissue regeneration process. Extensive research has been carried out to develop a compatible scaffold which mimic the anatomical site of injury and as well as accessing the stem cells and growth factors to home on the injured site. The present article provides an overview on different scaffold approaches and materials used to fabricate scaffolds, with their properties and associated advantages and disadvantages. In particular, the therapeutic potential of amniotic membrane and collagen scaffold has been extensively reviewed in here