TCP a ritrasmissione asimmetrica anticipata su WiFi

Nell'ambito dell'architettura RWMA per l'aumento della qualità del servizio in ambiente wireless, si colloca la ritrasmissione asimmetrica anticipata su wifi. Lo scopo è migliorare ed ottimizzare la comunicazione nel livello datalink tra Access Point e Nodo Mobile per quanto riguarda le connessioni TCP. Il progetto è sviluppato nell'ambiente simulativo OMNET++/INET.

Simulazione del protocollo TCP a ritrasmissione asimmetrica anticipata su WiFi

Progettazione e realizzazione di uno strumento simulativo che permette l'analisi degli effettivi vantaggi portati dalla ritrasmissione anticipata su WiFi applicata al protocollo TCP.

Analisi per via simulativa del protocollo tcp a ritrasmissione asimmetrica anticipata su wifi

Viene implementato un algoritmo di ritrasmissione dei pacchetti nel protocollo TCP. Lo studio viene fatt utilizzando il simulatore OMNET++ e il framework INET

TCP a ritrasmissione asimmetrica anticipata su Access Point WiFi

La perdita di pacchetti durante una trasmissione su una rete Wireless influisce in maniera fondamentale sulla qualità del collegamento tra due End-System. Lo scopo del progetto è quello di implementare una tecnica di ritrasmissione asimmetrica anticipata dei pacchetti perduti, in modo da minimizzare i tempi di recupero dati e migliorare la qualità della comunicazione. Partendo da uno studio su determinati tipi di ritrasmissione, in particolare quelli implementati dal progetto ABPS, Always Best Packet Switching, si è maturata l'idea che un tipo di ritrasmissione particolarmente utile potrebbe avvenire a livello Access Point: nel caso in cui la perdita di pacchetti avvenga tra l'AP e il nodo mobile che vi è collegato via IEEE802.11, invece che attendere la ritrasmissione TCP e Effettuata dall'End-System sorgente è lo stesso Access Point che e effettua una ritrasmissione verso il nodo mobile per permettere un veloce recupero dei dati perduti. Tale funzionalità stata quindi concettualmente divisa in due parti, la prima si riferisce all'applicazione che si occupa della bufferizzazione di pacchetti che attraversano l'AP e della loro copia in memoria per poi ritrasmetterli in caso di segnalazione di mancata acquisizione, la seconda riguardante la modifica al kernel che permette la segnalazione anticipata dell'errore. E' già stata sviluppata un'applicazione che prevede una ritrasmissione anticipata da parte dell'Access Point Wifi, cioè una ritrasmissione prima che la notifica di avvenuta perdita raggiunga l'end-point sorgente e appoggiata su un meccanismo di simulazione di Error Detection. Inoltre è stata anche realizzata la ritrasmissione asincrona e anticipata del TCP. Questo documento tratta della realizzazione di una nuova applicazione che fornisca una più effciente versione del buffer di pacchetti e utilizzi il meccanismo di una ritrasmissione asimmetrica e anticipata del TCP, cioè attivare la ritrasmissione su richiesta del TCP tramite notifiche di validità del campo Acknowledgement.

Modellazione e comparazione del protocollo TCP in scenari di mobilità

Nell'ultimo ventennio l'impatto delle tecnologie wireless ha rivoluzionato il modo di comunicare. Tuttavia oltre a svariati benefici sono emersi diversi problemi di integrazione e ottimizzazione. Uno tra i protocolli più conosciuto e utilizzato in ambito di comunicazioni di rete, il TCP, viene sempre più spesso usato all'interno di sistemi wireless, per le sue caratteristiche di affidabilità e controllo, senza però fornire supporto specifico. Ciò è materia di forte dibattito e ricerca, che mira a cercare di raffinare le differenti versioni di TCP per renderle wireless-oriented. In questo lavoro si analizzano due varianti di sistema che sfruttano il TCP in scenari di mobilità, una con TCP classico e l'altra con TCP modificato tramite l'aggiunta di un meccanismo di ritrasmissione anticipata, e se ne studiano i vari aspetti e comportamenti, valutandone le prestazioni per mezzo di metodi matematici consolidati in letteratura.

TCP-DR an effective protocol for infrastructure based wireless networks

TCP is a dominant protocol for consistent communication over the internet. It provides flow, congestion and error control mechanisms while using wired reliable networks. Its congestion control mechanism is not suitable for wireless links where data corruption and its lost rate are higher. The physical links are transparent from TCP that takes packet losses due to congestion only and initiates congestion handling mechanisms by reducing transmission speed. This results in wasting already limited available bandwidth on the wireless links. Therefore, there is no use to carry out research on increasing bandwidth of the wireless links until the available bandwidth is not optimally utilized. This paper proposed a hybrid scheme called TCP Detection and Recovery (TCP-DR) to distinguish congestion, corruption and mobility related losses and then instructs the data sending host to take appropriate action. Therefore, the link utilization is optimal while losses are either due to high bit error rate or mobility.

Differences between in vitro viability and differentiation and in vivo bone-forming efficacy of human mesenchymal stem cells cultured on PCL-TCP scaffolds

Human mesenchymal stem cells (hMSCs) possess great therapeutic potential for the treatment of bone disease and fracture non-union. Too often however, in vitro evidence alone of the interaction between hMSCs and the biomaterial of choice is used as justification for continued development of the material into the clinic. Clearly for hMSC-based regenerative medicine to be successful for the treatment of orthopaedic trauma, it is crucial to transplant hMSCs with a suitable carrier that facilitates their survival, optimal proliferation and osteogenic differentiation in vitro and in vivo. This motivated us to evaluate the use of polycaprolactone-20% tricalcium phosphate (PCL-TCP) scaffolds produced by fused deposition modeling for the delivery of hMSCs. When hMSCs were cultured on the PCL-TCP scaffolds and imaged by a combination of phase contrast, scanning electron and confocal laser microscopy, we observed five distinct stages of colonization over a 21-day period that were characterized by cell attachment, spreading, cellular bridging, the formation of a dense cellular mass and the accumulation of a mineralized extracellular matrix when induced with osteogenic stimulants. Having established that PCL-TCP scaffolds are able to support hMSC proliferation and osteogenic differentiation, we next tested the in vivo efficacy of hMSC-loaded PCL-TCP scaffolds in nude rat critical-sized femoral defects. We found that fluorescently labeled hMSCs survived in the defect site for up to 3 weeks post-transplantation. However, only 50% of the femoral defects treated with hMSCs responded favorably as determined by new bone volume. As such, we show that verification of hMSC viability and differentiation in vitro is not sufficient to predict the efficacy of transplanted stem cells to consistently promote bone formation in orthotopic defects in vivo.

Hylaluronan-based heparin-incorporated hydrogels for generation of axially vascularized bioartificial bone tissues : in vitro and in vivo evaluation in a PLDLLA-TCP-PCL-composite system

Smart matrices are required in bone tissueengineered grafts that provide an optimal environment for cells and retain osteo-inductive factors for sustained biological activity. We hypothesized that a slow-degrading heparin-incorporated hyaluronan (HA) hydrogel can preserve BMP-2; while an arterio–venous (A–V) loop can support axial vascularization to provide nutrition for a bioartificial bone graft. HA was evaluated for osteoblast growth and BMP-2 release. Porous PLDLLA–TCP–PCL scaffolds were produced by rapid prototyping technology and applied in vivo along with HA-hydrogel, loaded with either primary osteoblasts or BMP-2. A microsurgically created A–V loop was placed around the scaffold, encased in an isolation chamber in Lewis rats. HA-hydrogel supported growth of osteoblasts over 8 weeks and allowed sustained release of BMP-2 over 35 days. The A–V loop provided an angiogenic stimulus with the formation of vascularized tissue in the scaffolds. Bone-specific genes were detected by real time RT-PCR after 8 weeks. However, no significant amount of bone was observed histologically. The heterotopic isolation chamber in combination with absent biomechanical stimulation might explain the insufficient bone formation despite adequate expression of bone-related genes. Optimization of the interplay of osteogenic cells and osteo-inductive factors might eventually generate sufficient amounts of axially vascularized bone grafts for reconstructive surgery.

A comparative study of the proliferation and osteogenic differentiation of human periodontal ligament cells cultured on β-TCP ceramics and demineralized bone matrix with or without osteogenic inducers in vitro

The repair of bone defects that result from periodontal diseases remains a clinical challenge for periodontal therapy. β-tricalcium phosphate (β-TCP) ceramics are biodegradable inorganic bone substitutes with inorganic components that are similar to those of bone. Demineralized bone matrix (DBM) is an acid-extracted organic matrix derived from bone sources that consists of the collagen and matrix proteins of bone. A few studies have documented the effects of DBM on the proliferation and osteogenic differentiation of human periodontal ligament cells (hPDLCs). The aim of the present study was to investigate the effects of inorganic and organic elements of bone on the proliferation and osteogenic differentiation of hPDLCs using three-dimensional porous β-TCP ceramics and DBM with or without osteogenic inducers. Primary hPDLCs were isolated from human periodontal ligaments. The proliferation of the hPDLCs on the scaffolds in the growth culture medium was examined using a Cell‑Counting kit‑8 (CCK-8) and scanning electron microscopy (SEM). Alkaline phosphatase (ALP) activity and the osteogenic differentiation of the hPDLCs cultured on the β-TCP ceramics and DBM were examined in both the growth culture medium and osteogenic culture medium. Specific osteogenic differentiation markers were examined using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). SEM images revealed that the cells on the β-TCP were spindle-shaped and much more spread out compared with the cells on the DBM surfaces. There were no significant differences observed in cell proliferation between the β-TCP ceramics and the DBM scaffolds. Compared with the cells that were cultured on β-TCP ceramics, the ALP activity, as well as the Runx2 and osteocalcin (OCN) mRNA levels in the hPDLCs cultured on DBM were significantly enhanced both in the growth culture medium and the osteogenic culture medium. The organic elements of bone may exhibit greater osteogenic differentiation effects on hPDLCs than the inorganic elements.