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31 protocols using viscoat

1

Comparative Evaluation of Ocular Viscoelastic Devices

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Six OVDs were tested (table 1): Healon EndoCoat (Johnson & Johnson Vision Surgical, Santa Ana, CA, USA); Viscoat (Alcon Laboratories, Fort Worth, TX, USA); Methylvisc (Rayner Intraocular Lenses, Worthing, West Sussex, UK); Healon (Johnson & Johnson Vision Surgical); Healon GV (Johnson & Johnson Vision Surgical); and ProVisc (Alcon Laboratories).
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2

Phacoemulsification with Iris-Expanding Ring

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All Phaco procedures were performed by two surgeons using the temporal approach. Anesthesia was attained with topical proparacaine HCL 0.5% (Alcaine, Alcon Laboratories, Ft Worth, TX) or retrobulbar injection of 2% xylocaine. Preoperatively, phenylephrine HCl 5% plus tropicamide 0.5% (Sanmyd-P, Santen Inc., Osaka, Japan) was instilled every 5 min for 15 min into the operated eye and if at 30 min following start of dilation, pupil diameter remained at less than 5 mm, additional drops of 10% phenylephrine were applied.
Epinephrine 0.025%, lidocaine 0.75% and sodium chondroitin sulphate/sodium hyaluronate (Viscoat, Alcon Surgical, Ft Worth, TX) were sequentially injected into the anterior chamber (AC) through a paracentesis incision. A 2.4 mm temporal clear corneal incision (CCI) was created. Apparent posterior synechiae were released from the anterior lens capsule using capsulorrhexis forceps and various iris manipulating instruments. The AC was then additionally reformed with OVD and pupil diameter (PD) was measured to the nearest 0.5 mm using Castroviejo surgical calipers. For eyes with PD remaining less than 5.0 mm, the I-Ring was applied.
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3

Comparative Analysis of Ophthalmic Viscosurgical Devices

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Table 2 shows the OVDs used in this study. Opegan®, Opegan-Hi®, and Shellgan® were purchased from Santen Pharmaceutical Co., Ltd (Osaka, Japan). Opelead® was purchased from Senju Pharmaceutical Co., Ltd (Osaka, Japan). These four products are distributed in Japan. Viscoat® and Discovisc® were purchased from Alcon Inc. (Hünenberg, Switzerland), which are distributed worldwide. A 3% hyaluronic acid (HA) solution was prepared by dissolving HA powder (derived from chicken combs, Seikagaku Corp., Tokyo, Japan) in phosphate buffered saline at a final concentration of 3%.

OVD products investigated in this study

Bland nameCompositionDistributorMw (kDa)Classification [1 (link)]Apparent viscosity (Pa s)
HACS
Opegan1% HA with low MwSanten1100Very low viscosity dispersive5.1
Opelead1% HA with medium MwSenju1700Medium viscosity dispersive34.6
3% HA3% HA with low MwHomemade700Unreported35.2
Viscoat3% HA and 4% CSAlcon70020Medium viscosity dispersive61.7
Shellgan3% HA and 4% CSSanten70050Medium viscosity dispersive73.0
Discovisc1.65% HA and 4% CSAlcon160020Viscous dispersive117.0
Opegan-Hi1% HA with high MwSanten2500Viscous cohesive62.7

Molecular weights (Mw) of HA and chondroitin sulfate (CS) and apparent viscosity of OVDs at shear rate 1 (1/s) have already been determined [14 (link), 15 (link)]

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4

Corneal Patch Repair in Mini-Pigs

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Iodine (1mg/ml) and oxybuprokain (8mg/ml) were topically administrated to the eye, followed by injection of Viscoat (Alcon, Rødovre, Denmark) to the anterior chambers. A 2-mm in diameter full-thickness corneal perforation was made at the center of the eye of the mini-pig with a trephine. Subsequently, the corneal patch was used to seal the trephined corneal perforation. To patch the perforation, the center of the corneal patch was aligned to the center of the trephined wound to cover the perforation, followed by suturing with 12 nylon sutures (10–0) through the laser-made suture holes on the 12-hole patches. The sutures were made in order of rotational symmetry to keep the seal tight and balanced. After all the sutures were done, cefuroxim (1mg) was administered by intra-cameral injection, and a bandage contact lens was put in place to cover the sutured corneal patch.
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5

Phacoemulsification and IOL Insertion

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A single surgeon (CYP) performed phacoemulsification and intraocular lens (IOL) insertion. Under topical anesthesia, a side-port incision was made with a 1 mm diamond knife; then, the main clear corneal incision was made with a 2.8 mm diamond knife. An ophthalmic viscosurgical device, 4% chondroitin sulfate and 3% sodium hyaluronate (Viscoat, Alcon Laboratories, Fort Worth, TX, USA), was injected into the anterior chamber. Next, a continuous curvilinear capsulorhexis of 5 to 5.5 mm was created with a forcep. After hydrodissection with balanced salt solution, stop and chop phacoemulsification was performed using the Stellaris phacoemulsification machine (Bausch and Lomb, Rochester, NY, USA). An IOL (Tecnis IOL; Abbott Medical Optics, Santa Ana, CA, USA) was implanted within the capsular bag, and residual viscoelastic material was removed from the anterior chamber. After corneal stromal hydration on the main corneal incision with a balanced salt solution, the anterior chamber was reformed using a balanced salt solution. Postoperative medication was the same for all patients and consisted of topical 1% prednisolone and 0.5% levofloxacin 4 times per day for 4 weeks. Prostaglandin analogs were stopped after surgery for 3 months in the glaucoma patients who were treated with prostaglandin analog before surgery.
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6

Posterior Lamellar Keratoplasty Technique

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After local (retrobulbar anesthesia and a Nadbath facial nerve block), a 5.0-mm temporal corneal or corneoscleral incision was made. A 25G anterior chamber maintenance cannula was inserted in one side port. The recipient’s Descemet’s membrane was removed same as DMEK procedure. In most cases, the graft size was 7.75 mm or 8.0 mm. Pre-cut donor grafts were trephinated and the endothelial surface of the lenticle was coated with a small amount of viscoelastic material (Viscoat; Alcon). The donor tissue was gently inserted into the anterior chamber using a Busin glide (Asico) and Shimazaki DSAEK forceps (Inami, Tokyo, Japan). The pull-through technique was used to insert the donor graft. Air was carefully injected into the anterior chamber to unfold the graft. Fifteen minutes after the air injection, most of the air was replaced with balanced salt solution. Intraoperative and postoperative medication was the same as for DMEK.
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7

Corneal Transplant with Scleral Collarets

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Human corneal transplants with large scleral collarets and low endothelial cell densities were provided by the EFS Bourgogne Franche-Comté Cornea Bank (Besancon, France). The corneas were placed on an artificial chamber (Moria SA, Antony, France) (Fig. 2). A viscoelastic substance (Viscoat; Alcon) was injected posteriorly into the transplant to achieve an estimated intraocular pressure ranging between 10 and 20 mm Hg measured by digital palpation.
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8

Surgical Techniques for Astigmatism Reduction

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All surgeries were performed by the same experienced surgeon. The cylinder power and axis were calculated using the software provided by the manufacturers and taking into account the keratometric readings measured with a topographer. Phacoemulsification was performed through a 2.2-mm clear corneal incision. The astigmatism induced by the surgeon (FP) was previously known. The lenses were introduced via a 2.2-mm incision and the surgeon induced an astigmatism of 0.1 D in the right eye (temporal incision). In the left eye, the superior incision produced an astigmatism of 0.2 D. This was taken into account when the power of the lenses to be implanted was calculated.
In any case, it was necessary to open the incision for inserting the foldable IOL with the injector. To shield the corneal endothelial cells, a dispersive viscoelastic (Viscoat; Alcon Laboratories, Inc.) was first injected into the anterior chamber followed by another cohesive viscoelastic (Amvisc Plus; Bausch & Lomb) injected below the first one. The incision was not sutured and the eyes were not patched.
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9

Evaluating SPG-178's Resistance to Blood Diffusion

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To measure the ability of SPG-178 to resist the inward diffusion of blood, 2 ml of blood from a rabbit was placed in a 35-mm disposable petri dish after which 0.5 ml of SPG-178 was immersed within it. Photographs were taken immediately and 2 min after placement of the SPG-178, after which the images were digitized using Image J (NIH)20 . The area of blood ingress into the SPG-178 was quantitatively analyzed. The hyaluronic acid gel, Viscoat (Alcon, USA), was similarly tested as a comparator material commonly used in ophthalmic surgery.
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10

Preparing hiPSC-RPE Cell Sheets for Transplantation

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The method for creating the hiPSC-RPE cell sheets was described previously. 15 The hiPSC-RPE cell sheets were washed in PBS and transferred to a dish for a laser microdissection (LMD) (Lumox dish-35; Greiner, Graz, Austria). These sheets were kept moist with postconfluent medium or xeno-free and serum-free graft storage medium (DMEM phenol red free [Sigma-Aldrich Corp.], sodium pyruvate [Sigma-Aldrich Corp.], L-glutamine) (200 lL) until they were cut using LMD (PALM MicroBeam; Zeiss, Bernried, Germany) following the manufacturer's instructions and carried to the operation room. A graft storage medium with viscosity consisted of 50% graft storage medium and 50% ophthalmic viscosurgical device (Viscoat; Alcon, Abbott Park, IL, USA). The grafts measured 1.3 mm wide by 3.0 mm long except for a square of 0.65 mm wide by 0.65 mm long at one edge. After the grafts were carried to the operation room, aliquots of media (800 lL) were added to the dishes.
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