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16 protocols using dexamethasone (dex)

1

Extracapsular Lens Extraction in Sprague-Dawley Rats

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Sprague-Dawley rats of 10-week-old were used in this study. Intraperitoneal injection of 3.0% pentobarbital sodium was given to the rats to induce general anesthesia. The pupils were dilated with tropicamide phenylephrine eye drops (Santen, Osaka, Japan). In the extracapsular lens extraction (ECLE) model, a corneal incision was made with a 2.2 mm stab knife, and the anterior chamber was injected with sodium hyaluronate 1.5% (Qisheng Biologic Preparation, Shanghai, China). The anterior capsule was punctured with a discussion needle and the capsulorhexis was conducted with capsulorhexis forceps (MR-F212T-7, Mingren, Suzhou, China). The corneal incision was then extended to approximately 150 degrees with Vannas scissors, followed by hydrodissection and lens removal. Finally, the incision was closed with 10–0 sutures, and topical Tobradex ointment (0.3% tobramycin and 0.1% dexamethasone; Alcon Laboratories) was administered. The ECLE model of rats was only used in the electrophysiological experiment.
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2

Topical Treatment of Corneal Burns

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The topical solution of G. glabra extract (2% w/v) was prepared in normal saline using 10% dimethyl sulfoxide (DMSO) and a few drops of Tween-80 and mixed using vortex mixer. Similarly, glycyrrhizin (1% w/v) solution was prepared in normal saline. For preparation of the vehicle, dimethyl sulfoxide (DMSO) (10% v/v) and few drops of Tween-80 were mixed in normal saline. Dexamethasone (0.1%) (ALCON-COUVREUR, Belgium) was obtained from the local market and used as a positive control. All topical solutions were packed in special droppers purchased from the local market and stored at 4°C. Treatments were started on the 7th day of the corneal burns and continued for next 21 consecutive days. The eyes of different animal groups were topically treated with 3 drops of various solutions three times a day. The first group received treatment of G. glabra extract while second group was treated with glycyrrhizin. The third group was given the vehicle and the fourth group treated with Dexamethasone (0.1%) was considered as a positive control.
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3

Biodegradable PLGA Nanoparticle Formulation

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PLGA (lactic acid:glycolic acid = 50:50; i.v. = 48,000) was purchased from Evonik Industry (Essen, Germany). Dexamethasone and Nile red were purchased from Tokyo Chemical Industry (Tokyo, Japan). PVA (87–89% hydrolyzed), phosphate buffered saline (PBS) tablets, tween 80, trifluoroacetic acid (TFA; >99%), and calcium chloride dihydrate (>99%) were obtained from Merck (St. Louis, MO, USA). Dichloromethane (DCM; >99.5%), N,N-dimethylformamide (DMF; >99.5%), and acetone (>99.5%) were supplied by DaeJung (Siheung-si, Korea). Acetonitrile (ACN; >99.9%) was purchased from J.T. Bakers (Phillisburg, NJ, USA). PDMS (Sylgard 184) was obtained from Sewang Hitech Silicone (Bucheon-si, Korea). Alcaine® (0.5% proparacaine hydrochloride ophthalmic solution) and Maxidex® (0.1% Dexamethasone ophthalmic suspension) were purchased from Alcon-Couvreur (Fort Worth, TX, USA).
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4

Corneal Lenticule Implantation After SMILE

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All donor tissues were collected from the eye bank of the Hainan Eye Hospital in accordance with local guidelines (Hainan Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China). Topical anaesthesia consisted of proparacaine hydrochloride eye drops (Alcaine; Alcon Laboratories, Fort Worth, TX). A myopic correction of −0.75 diopters (28 μm thickness) using a femtosecond laser system under SMILE treatment was performed on the recipient cornea, and the surgical incision was 2.5 mm long. The surgeon unfolded the lenticule with microforceps and created a “stromal pocket” at a depth of 160 μm from the cornea epithelium, followed by implantation of the lenticule into the “stromal pocket.” The surgical procedures were detailed in our previous studies [13 (link), 16 (link)]. Following the surgery, all patients received tobramycin and dexamethasone (Alcon Laboratories, US) eye drops 4 times per day for 2 weeks and recombinant bovine basic fibroblast growth factor (Fusion Protein, Bausch and Lomb, Rochester, NY) eye gel 3 times per day for 6 months.
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5

Uncomplicated Cataract Surgery Protocol

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All patients underwent uncomplicated cataract surgery by two experienced cataract surgeons (Y.Z.L. and W.R.C.). General anesthesia was administered prior to surgery. After a temporal clear corneal incision was made, DuoVisc and a soft-shell technique were used to reform and stabilize the anterior chamber and protect the corneal endothelium. A 5.5–6.0 mm central continuous curvilinear capsulorhexis was created using a bent 26-gauge disposable needle. Hydro-dissection was performed using a balanced salt solution, and a standard phacoemulsification was performed to completely remove the lens. A 3-piece monofocal acrylic IOL with a 6.5-mm optic diameter (Sensar AR40e, AMO, Inc. CA, USA) was placed via in-the-bag implantation following lens removal.
Postoperative topical therapy included the administration of 0.3 % tobramycin and 0.1 % dexamethasone eye drops (Tobradex, Alcon Laboratories, Inc, Texas, USA) four times per day and 0.3 % tobramycin and 0.1 % dexamethasone eye ointment (Tobradex, Alcon Laboratories, Inc, Texas, USA) every night for 1 month.
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6

Postoperative Ocular Inflammation Management

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Tobradex (tobramycin 0.3% and dexamethasone 0.1%, Alcon, FortWorth, TX, USA) eyedrop was administered 4 times per day, followed by a weekly taper for 4 weeks thereafter, before shifting to 0.1% fluorometholone eye drops (Allergan, County Mayo, Ireland) 4 times per day followed by a weekly taper for 4 weeks. Preservative-free lubricants were used 4 times per day for 1 month. All patients were followed up daily for 1 week, weekly for 1 month, monthly for 3 months, and then at different intervals after surgery.
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7

Surgical Reconstruction of Ocular Surface Defects

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In both cases, the uHAM‐CCET construct was trimmed to match the wound size, placed with epithelium‐side‐up, and secured to the resected conjunctival margins with interrupted 10/0 polygalactin sutures and fibrin glue. All surgical steps were documented, including the preoperative size of the lesion (Fig. 1A), the positioning and tailoring of the uHAM‐CCET size after wound excision (Fig. 1B), and final aspect after suturing (Fig. 1C). The remaining uHAM‐CCET pieces were sent back to the laboratory, fixed, and processed for immunofluorescence and electron microscopies. Both patients were prescribed with dexamethasone (1 mg/ml, Alcon, Fort Worth, TX) and levofloxacin (1 mg/ml, Santen Pharmaceuticals, Osaka, Japan) eye drops four times daily for a minimum of 3 months.
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8

Rhesus Monkey SMILE Lenticule Implant

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Twelve rhesus monkeys were anaesthetized using an intramuscular injection of Zoletil 50 (5 mg/kg, Virbac). They then underwent SMILE surgery in one randomly selected eye to achieve a myopic treatment correction of −0.75 D. The following femtosecond laser parameters were used: 135 nJ, 160-μm cap thickness, 7.8-mm cap diameter, and 7.8-mm lamellar cornea diameter. A small incision was made at the 140° position with a side cut angle of 90°. The lenticule (28-μm thickness) was separated, and a space similar to a “stromal pocket” was produced (Fig. 2a). The graft was implanted in the “stromal pocket” (Fig. 2b). We avoided inverting the surface of the graft during implantation.

The procedure of implantation. a With SMILE surgery assisted, spread the lenticule out, producing a space like a ‘stromal pocket’. b Use forceps to implant the graft to the ‘stromal pocket’

Following the surgery, all monkeys received tobramycin and dexamethasone (Alcon Laboratories, US) eye drops 4 times per day for 1 week. We observed the ocular appearance of the monkeys every day and examined the 12 monkeys that received grafts at 1 week after implantation and 1, 3 and 6 months thereafter.
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9

Standardized Cataract Surgery Approach

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All cataract surgeries were performed using the phacoemulsification technique and the insertion of a foldable hydrophilic acrylic intraocular lens (AcrySof IQ IOL, Alcon, Inc.) in the capsular bag. A total of 0.3 mg TobraDex ointment (tobramycin 0.3% and dexamethasone 0.1%, Alcon, Inc.) was used at the end of the surgery in all patients. All patients were instructed to administer TobraDex eye drops (tobramycin 0.3% and dexamethasone 0.1%, Alcon, Inc.) 4 times daily for 2 weeks after surgery and 2 times daily until 4 weeks after cataract surgery. In addition, all patients were instructed to administer 0.1% Diclofenac sodium eye drops 4 times daily for 4 weeks after surgery. All patients were followed for at least 4 weeks after surgery.
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10

Fungal Keratitis Animal Model

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Levofloxacin eye drops (Santen, Osaka, Japan) were used in the experimental eyes twice a day for three days. Ten microliters of 2.4×106 CFU of the F. solanum spore suspension were injected into the corneal stroma with a microsyringe. TobraDex ophthalmic ointment (tobramycin 0.3%, dexamethasone 0.1%, Alcon) was dropped into the conjunctival sac and the eyelid was closed with a patch. Typical ulcer formation was observed on the third day and corneal fungus scrapings were identified as F. solanum, which are the criteria for successful establishment of animal models.
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