Objective To prepare the ephedrine chitosan-modified liposomes gels, detect the particle diameter and the entrapment efficiency, and investigate the transdermal diffusion characteristics in vitro. Methods Ephedrine liposomes suspensions were prepared using thin film evaporation and slowly dropped by 0.35% chitosan solution with pH values 5-6 in order to prepare the chitosan-modified liposomes gels. The particle diameter of the modified liposomes was detected by Laser Scattering Particle Size Distribution Analyzer. The entrapment efficiency was determined by reverse dialysis method with HPLC. Using Franz Diffusion Cell to investigate transdermal diffusion characteristics of the modified liposomes gels in vitro. Results The mean particle diameter of the modified liposome prepared was from 1 400 to 1 900 nm. The average entrapment efficiency of the modified liposomes was up to (41 ± 0.94)%. Ephedrine in the modified liposomes could penetrate rat skin. The results of the transdermal diffusion test showed the cumulative penetration amount of the ephedrine chitosan-modified liposomes gels was lower than that in the ephedrine solutions with time variation. Conclusion This preparatiom is prepared with simple technology and stable character. The entrapment efficiency of the ephedrine is higher and the assay method is simple and accurate. The penetrating rate of ephedrine is slow and the drug releasing is stable.

A lipopeptide compound was isolated from the culture of Bacillus subtilis HSO121 by methods of acidic precipitation, solvent extract, fractional precipitation, adsorption and prepared thin-layer chromatography; and its molecular structure was determined by by ninhydrin assay and IR methods following the Amino analysis, MS-MS and ESI-MS. It shows that the isolated lipopeptide consists of two homologues with molecular mass 1,022D and 1,036D and bearing a cyclic structure with the amino acid sequence Leu-Leu-Asp-Val-Leu-Leu-Glu in the peptide chain, which indicates that the isolated lipopeptide falls into the analogs of surfactin.

Humans ; Pleural Effusion ; etiology ; immunology ; T-Lymphocytes, Regulatory ; physiology

Objective: To study the direct and moderating effects of Esteem in the model of personality,shame and mental health. Corresponding factors in the whole model were extended. Methods: The SCL-90, EPQ-R Short Scale (EPQ-RS), Shame Scale and Esteem Scale were administered to 365 udergraduates (including 196 males and 169 females, mean age 20.65), and structural equation modeling method was used to study the direct and moderating effects of Esteem in the model. Results: The following conclusions are confirmed through model comparision: (1)Esteem has significant direct effect on the mental symptoms and shame in the model; (2)Esteem has significant moderating effect on the path of neuroticism to the mental symptoms in the model;(3)Psychoticism can independently affect the mental symptoms directly in the model. A new interactive perspective to the raltionship of shame and esteem was discussed in the end.

Objective To study the expression changes of matrix metalloproteinases (MMPs), protein kinase C (PKC) and nuclear factor-?B (NF-?B ) on the injured rabbit vascular smooth muscular cells (VSMC) transfected with tissue inhibitor of metalloproteinase-2 (TIMP-2) vector. Methods Lipofectin method was used to transfect TIMP-2 vector into VSMC, Western blot analysis to detect TIMP-2 peptides and zymography assay to determine MMPs. The activities of MMPs and NF-?B were detected by electrophoretic mobility shift assay (EMSA). The mRNA and protein expressions of PKC? were determined by RT-PCR and immunocytochemistry. Results The injured VSMC showed increased enzyme activity of MMP-2. There was very lower level expressions of PKC? and NF-?B in the normal VSMC but high in the injured VSMC. However, in injured VSMC transfected with TIMP-2 vector, the activity of MMP2/9 was suppressed and the expressions of PKC? and NF-?B decreased (P

Objective To investigate the effects of dexamethasone on the growth of cervical cancer induced by HeLa cells transplanted into BALB/c mice. Methods HeLa cells were inoculated subcutaneously into BALB/c mice. Dexamethasone (15 mg?kg-1?d-1) was injected intraperitoneally from the 6th or the 16th day after tumor inoculation for 10 days continuously. Diameter of tumors was measured every two or three days. Apoptotic bodies were observed by transmission electron microscopy and counted by TUNEL. Results Dexamethasone repressed the growth of cervical cancer and induced tumor cell apoptosis, but the tumor volumes were of statistical difference between the two groups of different injection start time (P

Objective To investigate the effects of over physiological dose of dexamethasone on cervical carcinoma cell xenografted tumors in nude mouse.Methods HeLa cells were inoculated subcutaneously in BALB/c female mice aged 5-6 weeks.Over physiological dose of dexamethasone(62.5 mg?kg-1?d-1) was injected into the peritoneum from the 16th day after inoculation for 10 d.Diameters of tumor were measured every two or three days.The volumes and the inhibition rates of tumor were calculated.Apoptotic bodies were observed by transmission electron microscopy and counted by TUNEL.VEGF and TNF-? were detected by immunohistochemistry.Results In vivo,over physiological dose of dexamethasone can repress the growth of tumor and induce cell apoptosis.Compared with the control group,the tumor sizes were significantly smaller(P0.05).Conclusion Over physiological dose of dexamethasone can repress cervical tumor growth in vivo.This action may be related to apoptosis and VEGF,but have no relationship with TNF-?.

An applied anatomical study on the blood supply of the flexor tendon was conducted in the upper extremities of fresh cadaver by means of arterial injection, transparence, maerodissection and histological preparation.The flexor digital tendon can be divided into two parts: non-synovial membrane part and synovial membrane part. The intrinsic vaseularization of non-synovial membrane part of the tendon which was wrapped in paratenon was major in the form of the longitudinal vascular bundles, while the transverse anastomotie branches were short and sparse. The vascularity of this part was simple and uniformly distributed. The intrinsic vascularity of the synovial part possessed distinct characteristics of segmentality and partiality. In the synovial sheath, the blood vessels distributed only onto the dorsal aspect, while the velar 1/3 to 1/2 of the tendon was devoid of vessels. The profundus and superfieialis tendons formed an avascular zone at the proximal interphalangeal and metacarpophalangeal joint separately. It was considered that the difference of the vascularization of tendon might be related to the mechanical force to which the tendon was subjected. The nutrition of tendon was discussed and the selection of tendon graft in the operation was suggested.

Objective:To investigate the expression of protein kinase C-?(PKC-?)in human ameloblastoma(AB)and its relationship with human telomerase reverse transcriptase(hTERT).Methods:The expression of hTERT mRNA was detected by in situ hybridization and PKC-? protein by immunohistochemistry in 54 cases of AB,7 cases of normal oral mucosa(NOM)and 16 cases of odontogenic keratocyst(OKC).Results:The positive rate of hTERT mRNA in AB,OKC and NOM was 94.4%(51/54),87.5%(14/16)and 14.3%(1/7)(P

Objective To compare the effect of two different dialysis modalities, hemodialysis (HD) and continuous ambulatory peritoneal dialysis (CAPD) on insulin resistance in patients with adult end-stage renal disease (ESRD), and to identify the possible predictive factors for insulin resistance. Methods Fifteen non-diabetic patients with ESRD (ESRD group) were selected. Eight patients were treated with HD (HD group), and 7 patients were treated with CAPD (CAPD group). The insulin inhibition was examined by hyper insulin-euglycemic glucose clamp technique before and after dialysis treatment, and the glucose disposal rate (GDR) was used as an index of insulin sensitivity during the clamp technique. Meanwhile, 8 healthy controls were selected as control group. The biochemical parameters which might be associated with insulin resistance were determined by multiple linear regression. Results The GDR in control group was (9.93 ± 1.33) mg/(kg · min), in ESRD group was (6.44 ± 1.76) mg/(kg·min), and there was statistical difference (P<0.05). The GDR in HD group after treatment was increased from (6.53 ± 1.84) mg/(kg · min) to (9.74 ± 2.88) mg/(kg · min), and there was statistical difference (P<0.01). The GDR in CAPD group after treatment was increased from (6.35 ± 1.65) mg/(kg·min) to (8.18 ± 1.76) mg/(kg·min), and there was statistical difference (P<0.05). Multiple linear regression result showed that the levels of urea nitrogen, hematocrit and bicarbonate were significant predictive factors in insulin resistance (P<0.05). Conclusions CAPD and HD therapy can improve insulin resistance in adult patients with ESRD.