2022
DOI: 10.1016/j.urolonc.2022.05.022
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A new catheter-integrated drug-delivery system for controlled intravesical mitomycin C release

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Cited by 8 publications
(11 citation statements)
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“…To compare how the ex-vivo porcine LUT model reflects catheterization in live animals, a recently established porcine model that facilitates catheterization in-vivo 19 , 28 was used. Although the ex-vivo tests were performed on male porcine LUTs, the in-vivo studies had to be performed in female pigs.…”
Section: Resultsmentioning
confidence: 99%
“…To compare how the ex-vivo porcine LUT model reflects catheterization in live animals, a recently established porcine model that facilitates catheterization in-vivo 19 , 28 was used. Although the ex-vivo tests were performed on male porcine LUTs, the in-vivo studies had to be performed in female pigs.…”
Section: Resultsmentioning
confidence: 99%
“…However, until now, urine specimens have been collected by either bladder catheterization or sterile bladder aspiration, which are both procedures that require the need for anaesthesia. [9][10][11][12] Although well-established protocols for shortterm anaesthesia exist, they often involve various combinations of opioids, benzodiazepines and alpha-2-agonists, which are associated with adverse effects such as obstipation, nausea, extended recovery, drug interactions or unwanted alterations in the animal's physiology that can interfere with the outcome of the study. [13][14][15] Therefore, the need for anaesthesia is a major limitation as it is not only stressful for the animal and increases procedural costs, but also limits the frequency of which urine specimens can be collected as daily anaesthesia for many days in a row is undesirable due to the concern for the animal's welfare.…”
Section: Introductionmentioning
confidence: 99%
“…In vitro results showed a sustained release of MMC for up to 12 days with an inhibitory effect against HTB-9 (ATCC bladder carcinoma cell line), but that time could be extended once the drug reservoir can be reloaded without removing the catheter. In vivo short-term studies were also performed in porcine models, and the therapeutic MMC concentration was released after 2 h. However, optimization of the system and longer pre-clinical studies are needed, as little or no MMC tissue uptake was observed [ 23 ].…”
Section: Fundamentalsmentioning
confidence: 99%